Linked Data
dbSNP Id:
rs779073856
ExAC:
1:68895482 G / A
gnomAD v2:
1-68895482-G-A
gnomAD v4:
1-68429799-G-A
MyVariant Identifiers:
chr1:g.68895482G>A (hg19)
chr1:g.68895482_68895483delinsAA (hg19)
chr1:g.68429799G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68429799G>A , CM000663.2:g.68429799G>A | GRCh38 |
| NC_000001.10:g.68895482G>A , CM000663.1:g.68895482G>A | GRCh37 |
| NC_000001.9:g.68668070G>A | NCBI36 |
| NG_008472.1:g.25161C>T | |
| NG_008472.2:g.25161C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1579C>T MANE Select | ENSP00000262340.5:p.His527Tyr | |
| ENST00000262340.5:c.1579C>T | ENSP00000262340.5:p.His527Tyr | |
| NM_000329.2:c.1579C>T | NP_000320.1:p.His527Tyr | |
| XM_017002027.1:c.1303C>T | XP_016857516.1:p.His435Tyr | |
| NM_000329.3:c.1579C>T MANE Select | NP_000320.1:p.His527Tyr |