Linked Data
ClinVar Variation Id:
2134942
ClinVar RCV Id:
RCV003048385
gnomAD v4:
2-21010190-G-A
MyVariant Identifiers:
chr2:g.21233062G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21010190G>A , CM000664.2:g.21010190G>A | GRCh38 |
| NC_000002.11:g.21233062G>A , CM000664.1:g.21233062G>A | GRCh37 |
| NC_000002.10:g.21086567G>A | NCBI36 |
| NG_011793.1:g.38884C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.6678C>T MANE Select | ENSP00000233242.1:p.Ile2226= | |
| ENST00000616098.4:c.6678C>T | ENSP00000477990.1:p.Ile2226= | |
| NM_000384.2:c.6678C>T | NP_000375.2:p.Ile2226= | |
| XM_011532809.1:c.5869+543C>T | XP_011531111.1:n.5869+543C>T | |
| NM_000384.3:c.6678C>T MANE Select | NP_000375.3:p.Ile2226= |