Linked Data
ClinVar Variation Id:
1799530
dbSNP Id:
rs766819324
ExAC:
2:26697477 G / C
gnomAD v2:
2-26697477-G-C
gnomAD v4:
2-26474609-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26474609G>C , CM000664.2:g.26474609G>C | GRCh38 |
| NC_000002.11:g.26697477G>C , CM000664.1:g.26697477G>C | GRCh37 |
| NC_000002.10:g.26550981G>C | NCBI36 |
| NG_009937.1:g.89090C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272371.7:c.3192C>G MANE Select | ENSP00000272371.2:p.Tyr1064Ter | |
| ENST00000339598.8:c.951C>G MANE Plus Clinical | ENSP00000344521.3:p.Tyr317Ter | |
| ENST00000402415.8:c.951C>G | ENSP00000383906.4:p.Tyr317Ter | |
| ENST00000272371.6:c.3192C>G | ENSP00000272371.2:p.Tyr1064Ter | |
| ENST00000338581.10:c.951C>G | ENSP00000345137.6:p.Tyr317Ter | |
| ENST00000339598.7:c.951C>G | ENSP00000344521.3:p.Tyr317Ter | |
| ENST00000402415.7:c.1122C>G | ENSP00000383906.3:p.Tyr374Ter | |
| ENST00000403946.7:c.3192C>G | ENSP00000385255.3:p.Tyr1064Ter | |
| NM_001287489.1:c.3192C>G | NP_001274418.1:p.Tyr1064Ter | |
| NM_004802.3:c.951C>G | NP_004793.2:p.Tyr317Ter | |
| NM_194248.2:c.3192C>G | NP_919224.1:p.Tyr1064Ter | |
| NM_194322.2:c.1122C>G | NP_919303.1:p.Tyr374Ter | |
| NM_194323.2:c.951C>G | NP_919304.1:p.Tyr317Ter | |
| XM_005264644.2:c.3237C>G | XP_005264701.1:p.Tyr1079Ter | |
| XM_011533185.1:c.3237C>G | XP_011531487.1:p.Tyr1079Ter | |
| XM_017005338.1:c.3192C>G | XP_016860827.1:p.Tyr1064Ter | |
| NM_001287489.2:c.3192C>G | NP_001274418.1:p.Tyr1064Ter | |
| NM_004802.4:c.951C>G | NP_004793.2:p.Tyr317Ter | |
| NM_194248.3:c.3192C>G MANE Select | NP_919224.1:p.Tyr1064Ter | |
| NM_194322.3:c.1122C>G | NP_919303.1:p.Tyr374Ter | |
| NM_194323.3:c.951C>G MANE Plus Clinical | NP_919304.1:p.Tyr317Ter |