Linked Data
dbSNP Id:
rs1293905664
gnomAD v2:
7-98021256-G-A
gnomAD v3:
7-98391944-G-A
gnomAD v4:
7-98391944-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.98391944G>A , CM000669.2:g.98391944G>A | GRCh38 |
| NC_000007.13:g.98021256G>A , CM000669.1:g.98021256G>A | GRCh37 |
| NC_000007.12:g.97859192G>A | NCBI36 |
| NG_013090.1:g.14172C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000005260.9:c.51+8858C>T MANE Select | ENSP00000005260.8:n.51+8858C>T | |
| ENST00000005260.8:c.51+8858C>T | ENSP00000005260.8:n.51+8858C>T | |
| ENST00000462558.5:n.267+8858C>T | ||
| ENST00000479789.1:n.357+8037C>T | ||
| NM_018842.4:c.51+8858C>T | NP_061330.2:n.51+8858C>T | |
| NM_018842.5:c.51+8858C>T MANE Select | NP_061330.2:n.51+8858C>T |