MyVariant.info:
GRCh37
chr10:g.73567096G>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.71807339G>A , CM000672.2:g.71807339G>A | GRCh38 |
| NC_000010.10:g.73567096G>A , CM000672.1:g.73567096G>A | GRCh37 |
| NC_000010.9:g.73237102G>A | NCBI36 |
| NG_008835.1:g.415393G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000224721.12:c.8241G>A MANE Select | ENSP00000224721.9:p.Val2747= | |
| ENST00000642965.1:c.2174G>A | ENSP00000495222.1:n.2174G>A | |
| ENST00000647092.1:c.1838G>A | ENSP00000495176.1:n.1838G>A | |
| ENST00000224721.10:c.8256G>A | ENSP00000224721.8:p.Val2752= | |
| ENST00000398788.4:c.1521G>A | ENSP00000381768.3:p.Val507= | |
| ENST00000475158.1:n.1777G>A | ||
| ENST00000619887.4:c.1521G>A | ENSP00000478374.1:p.Val507= | |
| ENST00000622827.4:c.8241G>A | ENSP00000483211.1:p.Val2747= | |
| NM_001171933.1:c.1521G>A | NP_001165404.1:p.Val507= | |
| NM_001171934.1:c.1521G>A | NP_001165405.1:p.Val507= | |
| NM_022124.5:c.8241G>A | NP_071407.4:p.Val2747= | |
| XM_006717940.2:c.8436G>A | XP_006718003.1:p.Val2812= | |
| XM_006717942.2:c.8370G>A | XP_006718005.1:p.Val2790= | |
| XM_011540039.1:c.8433G>A | XP_011538341.1:p.Val2811= | |
| XM_011540040.1:c.8430G>A | XP_011538342.1:p.Val2810= | |
| XM_011540041.1:c.8376G>A | XP_011538343.1:p.Val2792= | |
| XM_011540042.1:c.8346G>A | XP_011538344.1:p.Val2782= | |
| XM_011540043.1:c.8436G>A | XP_011538345.1:p.Val2812= | |
| XM_011540044.1:c.8301G>A | XP_011538346.1:p.Val2767= | |
| XM_011540045.1:c.8436G>A | XP_011538347.1:p.Val2812= | |
| XM_011540046.1:c.7896G>A | XP_011538348.1:p.Val2632= | |
| XM_011540047.1:c.7254G>A | XP_011538349.1:p.Val2418= | |
| XM_011540052.1:c.4764G>A | XP_011538354.1:p.Val1588= | |
| NM_022124.6:c.8241G>A MANE Select | NP_071407.4:p.Val2747= |