Linked Data
ClinVar Variation Id:
1478759
ClinVar RCV Id:
RCV001990771
dbSNP Id:
rs199475619
ExAC:
12:103306580 G / T
gnomAD v2:
12-103306580-G-T
gnomAD v3:
12-102912802-G-T
gnomAD v4:
12-102912802-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102912802G>T , CM000674.2:g.102912802G>T | GRCh38 |
| NC_000012.11:g.103306580G>T , CM000674.1:g.103306580G>T | GRCh37 |
| NC_000012.10:g.101830710G>T | NCBI36 |
| NG_008690.1:g.9801C>A | |
| NG_008690.2:g.50609C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.157C>A MANE Select | ENSP00000448059.1:p.Arg53Ser | |
| ENST00000307000.7:c.142C>A | ENSP00000303500.2:p.Arg48Ser | |
| ENST00000546844.1:c.157C>A | ENSP00000446658.1:p.Arg53Ser | |
| ENST00000548677.2:n.244C>A | ||
| ENST00000548928.1:n.79C>A | ||
| ENST00000549111.5:n.253C>A | ||
| ENST00000550978.6:c.141C>A | ||
| ENST00000551337.5:c.157C>A | ENSP00000447620.1:p.Arg53Ser | |
| ENST00000551988.5:n.246C>A | ||
| ENST00000553106.5:c.157C>A | ENSP00000448059.1:p.Arg53Ser | |
| ENST00000635500.1:n.125C>A | ||
| NM_000277.1:c.157C>A | NP_000268.1:p.Arg53Ser | |
| XM_011538422.1:c.157C>A | XP_011536724.1:p.Arg53Ser | |
| NM_000277.2:c.157C>A | NP_000268.1:p.Arg53Ser | |
| NM_001354304.1:c.157C>A | NP_001341233.1:p.Arg53Ser | |
| XM_017019370.2:c.157C>A | XP_016874859.1:p.Arg53Ser | |
| NM_000277.3:c.157C>A MANE Select | NP_000268.1:p.Arg53Ser | |
| NM_001354304.2:c.157C>A | NP_001341233.1:p.Arg53Ser |