Linked Data
dbSNP Id:
rs1339197
gnomAD v2:
6-128608211-G-A
gnomAD v3:
6-128287066-G-A
gnomAD v4:
6-128287066-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.128287066G>A , CM000668.2:g.128287066G>A | GRCh38 |
| NC_000006.11:g.128608211G>A , CM000668.1:g.128608211G>A | GRCh37 |
| NC_000006.10:g.128649904G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000368226.9:c.495+34973C>T MANE Select | ENSP00000357209.4:n.495+34973C>T | |
| ENST00000368207.7:c.495+34973C>T | ENSP00000357190.3:n.495+34973C>T | |
| ENST00000368210.7:c.495+34973C>T | ENSP00000357193.3:n.495+34973C>T | |
| ENST00000368213.9:c.495+34973C>T | ENSP00000357196.5:n.495+34973C>T | |
| ENST00000368215.7:c.495+34973C>T | ENSP00000357198.3:n.495+34973C>T | |
| ENST00000368226.8:c.495+34973C>T | ENSP00000357209.4:n.495+34973C>T | |
| ENST00000429595.1:n.135+34973C>T | ||
| ENST00000490332.2:c.143+34973C>T | ||
| ENST00000495748.5:n.521+34973C>T | ||
| ENST00000524481.5:n.736+34973C>T | ||
| ENST00000524534.5:n.652+34973C>T | ||
| ENST00000531050.5:c.53-44464C>T | ENSP00000432960.1:n.53-44464C>T | |
| ENST00000532331.5:c.495+34973C>T | ENSP00000432973.1:n.495+34973C>T | |
| NM_001135648.2:c.495+34973C>T | NP_001129120.1:n.495+34973C>T | |
| NM_001291981.1:c.495+34973C>T | NP_001278910.1:n.495+34973C>T | |
| NM_001291982.1:c.495+34973C>T | NP_001278911.1:n.495+34973C>T | |
| NM_001291983.1:c.109-44464C>T | NP_001278912.1:n.109-44464C>T | |
| NM_001291984.1:c.495+34973C>T | NP_001278913.1:n.495+34973C>T | |
| NM_002844.3:c.495+34973C>T | NP_002835.2:n.495+34973C>T | |
| XM_006715537.1:c.495+34973C>T | XP_006715600.1:n.495+34973C>T | |
| XM_011536014.1:c.495+34973C>T | XP_011534316.1:n.495+34973C>T | |
| XM_011536015.1:c.495+34973C>T | XP_011534317.1:n.495+34973C>T | |
| XM_011536016.1:c.495+34973C>T | XP_011534318.1:n.495+34973C>T | |
| XM_011536017.1:c.282+34973C>T | XP_011534319.1:n.282+34973C>T | |
| XM_011536018.1:c.282+34973C>T | XP_011534320.1:n.282+34973C>T | |
| XM_011536020.1:c.495+34973C>T | XP_011534322.1:n.495+34973C>T | |
| XM_011536021.1:c.495+34973C>T | XP_011534323.1:n.495+34973C>T | |
| XM_006715537.3:c.495+34973C>T | XP_006715600.1:n.495+34973C>T | |
| XM_011536014.3:c.495+34973C>T | XP_011534316.1:n.495+34973C>T | |
| XM_011536015.3:c.495+34973C>T | XP_011534317.1:n.495+34973C>T | |
| XM_011536016.3:c.495+34973C>T | XP_011534318.1:n.495+34973C>T | |
| XM_011536017.3:c.282+34973C>T | XP_011534319.1:n.282+34973C>T | |
| XM_011536018.2:c.282+34973C>T | XP_011534320.1:n.282+34973C>T | |
| XM_011536020.3:c.495+34973C>T | XP_011534322.1:n.495+34973C>T | |
| XM_011536021.3:c.495+34973C>T | XP_011534323.1:n.495+34973C>T | |
| XM_017011145.1:c.282+34973C>T | XP_016866634.1:n.282+34973C>T | |
| XM_017011146.1:c.282+34973C>T | XP_016866635.1:n.282+34973C>T | |
| XM_017011147.1:c.282+34973C>T | XP_016866636.1:n.282+34973C>T | |
| XM_017011148.1:c.282+34973C>T | XP_016866637.1:n.282+34973C>T | |
| NM_001135648.3:c.495+34973C>T | NP_001129120.1:n.495+34973C>T | |
| NM_001291981.2:c.495+34973C>T | NP_001278910.1:n.495+34973C>T | |
| NM_001291982.2:c.495+34973C>T | NP_001278911.1:n.495+34973C>T | |
| NM_001291983.2:c.109-44464C>T | NP_001278912.1:n.109-44464C>T | |
| NM_001291984.2:c.495+34973C>T | NP_001278913.1:n.495+34973C>T | |
| NM_002844.4:c.495+34973C>T MANE Select | NP_002835.2:n.495+34973C>T |