Linked Data
ClinVar Variation Id:
1668112
ClinVar RCV Id:
RCV002191613
dbSNP Id:
rs758216516
ExAC:
3:52356572 G / A
gnomAD v2:
3-52356572-G-A
gnomAD v3:
3-52322556-G-A
gnomAD v4:
3-52322556-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52322556G>A , CM000665.2:g.52322556G>A | GRCh38 |
| NC_000003.11:g.52356572G>A , CM000665.1:g.52356572G>A | GRCh37 |
| NC_000003.10:g.52331612G>A | NCBI36 |
| NG_052911.1:g.11238G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000420323.7:c.114G>A MANE Select | ENSP00000401514.2:p.Pro38= | |
| ENST00000420323.6:c.114G>A | ENSP00000401514.2:p.Pro38= | |
| ENST00000486752.5:n.375G>A | ||
| ENST00000497875.1:n.279G>A | ||
| NM_015512.4:c.114G>A | NP_056327.4:p.Pro38= | |
| XM_011533577.1:c.114G>A | XP_011531879.1:p.Pro38= | |
| XM_017006129.1:c.114G>A | XP_016861618.1:p.Pro38= | |
| XM_017006130.1:c.114G>A | XP_016861619.1:p.Pro38= | |
| XM_017006131.1:c.114G>A | XP_016861620.1:p.Pro38= | |
| XM_017006132.1:c.114G>A | XP_016861621.1:p.Pro38= | |
| XM_017006133.1:c.114G>A | XP_016861622.1:p.Pro38= | |
| XR_001740098.1:n.3263G>A | ||
| XR_001740099.1:n.3263G>A | ||
| NM_015512.5:c.114G>A MANE Select | NP_056327.4:p.Pro38= |