Linked Data
dbSNP Id:
rs775615275
ExAC:
7:42005794 C / A
gnomAD v2:
7-42005794-C-A
gnomAD v4:
7-41966196-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41966196C>A , CM000669.2:g.41966196C>A | GRCh38 |
| NC_000007.13:g.42005794C>A , CM000669.1:g.42005794C>A | GRCh37 |
| NC_000007.12:g.41972319C>A | NCBI36 |
| NG_008434.1:g.275825G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395925.8:c.2877G>T MANE Select | ENSP00000379258.3:p.Leu959= | |
| ENST00000677288.1:c.2703G>T | ENSP00000503986.1:p.Leu901= | |
| ENST00000677605.1:c.2877G>T | ENSP00000503743.1:p.Leu959= | |
| ENST00000678429.1:c.2877G>T | ENSP00000502957.1:p.Leu959= | |
| ENST00000395925.7:c.2877G>T | ENSP00000379258.3:p.Leu959= | |
| ENST00000479210.1:n.2854G>T | ||
| NM_000168.5:c.2877G>T | NP_000159.3:p.Leu959= | |
| XM_005249703.1:c.2877G>T | XP_005249760.1:p.Leu959= | |
| XM_005249704.2:c.2877G>T | XP_005249761.1:p.Leu959= | |
| XM_011515272.1:c.2877G>T | XP_011513574.1:p.Leu959= | |
| XM_011515273.1:c.2877G>T | XP_011513575.1:p.Leu959= | |
| XM_011515274.1:c.2700G>T | XP_011513576.1:p.Leu900= | |
| XM_011515274.2:c.2700G>T | XP_011513576.1:p.Leu900= | |
| XM_017011997.1:c.2874G>T | XP_016867486.1:p.Leu958= | |
| NM_000168.6:c.2877G>T MANE Select | NP_000159.3:p.Leu959= |