Linked Data
ClinVar Variation Id:
2940617
ClinVar RCV Id:
RCV003799927
MyVariant Identifiers:
chr2:g.21233515C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21010643C>T , CM000664.2:g.21010643C>T | GRCh38 |
| NC_000002.11:g.21233515C>T , CM000664.1:g.21233515C>T | GRCh37 |
| NC_000002.10:g.21087020C>T | NCBI36 |
| NG_011793.1:g.38431G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.6225G>A MANE Select | ENSP00000233242.1:p.Glu2075= | |
| ENST00000616098.4:c.6225G>A | ENSP00000477990.1:p.Glu2075= | |
| NM_000384.2:c.6225G>A | NP_000375.2:p.Glu2075= | |
| XM_011532809.1:c.5869+90G>A | XP_011531111.1:n.5869+90G>A | |
| NM_000384.3:c.6225G>A MANE Select | NP_000375.3:p.Glu2075= |