Linked Data
dbSNP Id:
rs774492565
ExAC:
11:17574745 G / A
gnomAD v2:
11-17574745-G-A
gnomAD v3:
11-17553198-G-A
gnomAD v4:
11-17553198-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17553198G>A , CM000673.2:g.17553198G>A | GRCh38 |
| NC_000011.9:g.17574745G>A , CM000673.1:g.17574745G>A | GRCh37 |
| NC_000011.8:g.17531321G>A | NCBI36 |
| NG_033191.1:g.10826G>A | |
| NG_033191.2:g.10826G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399391.7:c.408G>A | ENSP00000382323.2:p.Pro136= | |
| ENST00000399397.6:c.372G>A MANE Select | ENSP00000382329.2:p.Pro124= | |
| ENST00000399391.6:c.408G>A | ENSP00000382323.2:p.Pro136= | |
| ENST00000399397.5:c.372G>A | ENSP00000382329.2:p.Pro124= | |
| ENST00000428619.1:c.189G>A | ENSP00000399057.2:p.Pro63= | |
| ENST00000498332.5:n.278G>A | ||
| NM_001277269.1:c.408G>A | NP_001264198.1:p.Pro136= | |
| NM_001292063.1:c.372G>A | NP_001278992.1:p.Pro124= | |
| NM_001277269.2:c.408G>A | NP_001264198.1:p.Pro136= | |
| NM_001292063.2:c.372G>A MANE Select | NP_001278992.1:p.Pro124= |