Linked Data
dbSNP Id:
rs35460572
ExAC:
Y:14968449 A / G
gnomAD v2:
Y-14968449-A-G
gnomAD v3:
Y-12856524-A-G
gnomAD v4:
Y-12856524-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12856524A>G , CM000686.2:g.12856524A>G | GRCh38 |
| NC_000024.9:g.14968449A>G , CM000686.1:g.14968449A>G | GRCh37 |
| NC_000024.8:g.13477843A>G | NCBI36 |
| NG_008311.1:g.160290A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651177.1:c.7221+28A>G | ENSP00000498372.1:n.7221+28A>G | |
| ENST00000338981.7:c.7221+28A>G MANE Select | ENSP00000342812.3:n.7221+28A>G | |
| ENST00000426564.6:n.7248+28A>G | ||
| ENST00000453031.1:c.266+28A>G | ||
| NM_004654.3:c.7221+28A>G | NP_004645.2:n.7221+28A>G | |
| XM_011531469.1:c.7221+28A>G | XP_011529771.1:n.7221+28A>G | |
| XM_011531470.1:c.6987+28A>G | XP_011529772.1:n.6987+28A>G | |
| XM_017030078.2:c.7236+28A>G | XP_016885567.1:n.7236+28A>G | |
| NM_004654.4:c.7221+28A>G MANE Select | NP_004645.2:n.7221+28A>G |