Linked Data
ClinVar Variation Id:
2039562
ClinVar RCV Id:
RCV002907913
dbSNP Id:
rs375673789
gnomAD v2:
7-42005461-G-T
gnomAD v3:
7-41965863-G-T
gnomAD v4:
7-41965863-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41965863G>T , CM000669.2:g.41965863G>T | GRCh38 |
| NC_000007.13:g.42005461G>T , CM000669.1:g.42005461G>T | GRCh37 |
| NC_000007.12:g.41971986G>T | NCBI36 |
| NG_008434.1:g.276158C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395925.8:c.3210C>A MANE Select | ENSP00000379258.3:p.Thr1070= | |
| ENST00000677288.1:c.3036C>A | ENSP00000503986.1:p.Thr1012= | |
| ENST00000677605.1:c.3210C>A | ENSP00000503743.1:p.Thr1070= | |
| ENST00000678429.1:c.3210C>A | ENSP00000502957.1:p.Thr1070= | |
| ENST00000395925.7:c.3210C>A | ENSP00000379258.3:p.Thr1070= | |
| ENST00000479210.1:n.3187C>A | ||
| NM_000168.5:c.3210C>A | NP_000159.3:p.Thr1070= | |
| XM_005249703.1:c.3210C>A | XP_005249760.1:p.Thr1070= | |
| XM_005249704.2:c.3210C>A | XP_005249761.1:p.Thr1070= | |
| XM_011515272.1:c.3210C>A | XP_011513574.1:p.Thr1070= | |
| XM_011515273.1:c.3210C>A | XP_011513575.1:p.Thr1070= | |
| XM_011515274.1:c.3033C>A | XP_011513576.1:p.Thr1011= | |
| XM_011515274.2:c.3033C>A | XP_011513576.1:p.Thr1011= | |
| XM_017011997.1:c.3207C>A | XP_016867486.1:p.Thr1069= | |
| NM_000168.6:c.3210C>A MANE Select | NP_000159.3:p.Thr1070= |