Linked Data
dbSNP Id:
rs192993096
gnomAD v2:
7-146489513-C-T
gnomAD v3:
7-146792421-C-T
gnomAD v4:
7-146792421-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.146792421C>T , CM000669.2:g.146792421C>T | GRCh38 |
| NC_000007.13:g.146489513C>T , CM000669.1:g.146489513C>T | GRCh37 |
| NC_000007.12:g.146120446C>T | NCBI36 |
| NG_007092.2:g.681061C>T | |
| NG_007092.3:g.681421C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361727.8:c.208+18040C>T MANE Select | ENSP00000354778.3:n.208+18040C>T | |
| ENST00000636561.1:n.111+18040C>T | ||
| ENST00000637150.1:n.137+18040C>T | ||
| ENST00000637694.1:n.111+18040C>T | ||
| ENST00000638117.1:n.111+18040C>T | ||
| ENST00000361727.7:c.208+18040C>T | ENSP00000354778.3:n.208+18040C>T | |
| ENST00000625365.2:c.208+18040C>T | ENSP00000485955.1:n.208+18040C>T | |
| NM_014141.5:c.208+18040C>T | NP_054860.1:n.208+18040C>T | |
| XM_017011950.2:c.208+18040C>T | XP_016867439.1:n.208+18040C>T | |
| NM_014141.6:c.208+18040C>T MANE Select | NP_054860.1:n.208+18040C>T |