Linked Data
dbSNP Id:
rs189942526
gnomAD v2:
9-104187021-G-A
gnomAD v3:
9-101424739-G-A
gnomAD v4:
9-101424739-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101424739G>A , CM000671.2:g.101424739G>A | GRCh38 |
| NC_000009.11:g.104187021G>A , CM000671.1:g.104187021G>A | GRCh37 |
| NC_000009.10:g.103226842G>A | NCBI36 |
| NG_012387.1:g.16042C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647789.2:c.999+104C>T MANE Select | ENSP00000497767.1:n.999+104C>T | |
| ENST00000648064.1:c.999+104C>T | ENSP00000497990.1:n.999+104C>T | |
| ENST00000648758.1:c.999+104C>T | ENSP00000497731.1:n.999+104C>T | |
| ENST00000649902.1:c.*74C>T | ENSP00000497216.1:n.*74C>T | |
| ENST00000374855.8:c.999+104C>T | ENSP00000363988.4:n.999+104C>T | |
| ENST00000616752.1:c.*11+104C>T | ENSP00000481363.1:n.*11+104C>T | |
| NM_000035.3:c.999+104C>T | NP_000026.2:n.999+104C>T | |
| NM_000035.4:c.999+104C>T MANE Select | NP_000026.2:n.999+104C>T |