Linked Data
dbSNP Id:
rs1392895242
gnomAD v2:
6-25812963-G-A
gnomAD v3:
6-25812735-G-A
gnomAD v4:
6-25812735-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.25812735G>A , CM000668.2:g.25812735G>A | GRCh38 |
| NC_000006.11:g.25812963G>A , CM000668.1:g.25812963G>A | GRCh37 |
| NC_000006.10:g.25920942G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000244527.10:c.897+96C>T MANE Select | ENSP00000244527.4:n.897+96C>T | |
| ENST00000244527.8:c.897+96C>T | ENSP00000244527.4:n.897+96C>T | |
| ENST00000377886.6:c.*148+96C>T | ENSP00000367118.2:n.*148+96C>T | |
| ENST00000468082.1:c.735+360C>T | ENSP00000420546.1:n.735+360C>T | |
| ENST00000476801.5:c.897+96C>T | ENSP00000420614.1:n.897+96C>T | |
| NM_005074.3:c.897+96C>T | NP_005065.2:n.897+96C>T | |
| XM_011514818.1:c.897+96C>T | XP_011513120.1:n.897+96C>T | |
| XM_011514819.1:c.810+96C>T | XP_011513121.1:n.810+96C>T | |
| XM_011514820.1:c.735+360C>T | XP_011513122.1:n.735+360C>T | |
| XM_011514821.1:c.684+96C>T | XP_011513123.1:n.684+96C>T | |
| XM_011514818.2:c.1047+96C>T | XP_011513120.2:n.1047+96C>T | |
| XM_011514819.2:c.960+96C>T | XP_011513121.2:n.960+96C>T | |
| XM_011514820.2:c.885+360C>T | XP_011513122.2:n.885+360C>T | |
| XM_011514821.2:c.684+96C>T | XP_011513123.1:n.684+96C>T | |
| XM_017011199.1:c.1047+96C>T | XP_016866688.1:n.1047+96C>T | |
| XM_017011200.1:c.1047+96C>T | XP_016866689.1:n.1047+96C>T | |
| XM_017011201.2:c.1047+96C>T | XP_016866690.1:n.1047+96C>T | |
| XM_017011202.1:c.963+96C>T | XP_016866691.1:n.963+96C>T | |
| NM_005074.5:c.897+96C>T MANE Select | NP_005065.2:n.897+96C>T |