Linked Data
ClinVar Variation Id:
650381
ClinVar RCV Id:
RCV000805522
dbSNP Id:
rs767453024
ExAC:
12:103288642 C / T
gnomAD v2:
12-103288642-C-T
gnomAD v3:
12-102894864-C-T
gnomAD v4:
12-102894864-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102894864C>T , CM000674.2:g.102894864C>T | GRCh38 |
| NC_000012.11:g.103288642C>T , CM000674.1:g.103288642C>T | GRCh37 |
| NC_000012.10:g.101812772C>T | NCBI36 |
| NG_008690.1:g.27739G>A | |
| NG_008690.2:g.68547G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.223G>A MANE Select | ENSP00000448059.1:p.Asp75Asn | |
| ENST00000307000.7:c.208G>A | ENSP00000303500.2:p.Asp70Asn | |
| ENST00000546844.1:c.223G>A | ENSP00000446658.1:p.Asp75Asn | |
| ENST00000548677.2:n.310G>A | ||
| ENST00000548928.1:n.145G>A | ||
| ENST00000549111.5:n.319G>A | ||
| ENST00000550978.6:c.207G>A | ||
| ENST00000551337.5:c.223G>A | ENSP00000447620.1:p.Asp75Asn | |
| ENST00000551988.5:n.312G>A | ||
| ENST00000553106.5:c.223G>A | ENSP00000448059.1:p.Asp75Asn | |
| NM_000277.1:c.223G>A | NP_000268.1:p.Asp75Asn | |
| XM_011538422.1:c.223G>A | XP_011536724.1:p.Asp75Asn | |
| NM_000277.2:c.223G>A | NP_000268.1:p.Asp75Asn | |
| NM_001354304.1:c.223G>A | NP_001341233.1:p.Asp75Asn | |
| XM_017019370.2:c.223G>A | XP_016874859.1:p.Asp75Asn | |
| NM_000277.3:c.223G>A MANE Select | NP_000268.1:p.Asp75Asn | |
| NM_001354304.2:c.223G>A | NP_001341233.1:p.Asp75Asn |