Linked Data
ClinVar Variation Id:
3231429
ClinVar RCV Id:
RCV004525500
MyVariant Identifiers:
chr2:g.21234181T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21011309T>A , CM000664.2:g.21011309T>A | GRCh38 |
| NC_000002.11:g.21234181T>A , CM000664.1:g.21234181T>A | GRCh37 |
| NC_000002.10:g.21087686T>A | NCBI36 |
| NG_011793.1:g.37765A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.5559A>T MANE Select | ENSP00000233242.1:p.Ala1853= | |
| ENST00000616098.4:c.5559A>T | ENSP00000477990.1:p.Ala1853= | |
| NM_000384.2:c.5559A>T | NP_000375.2:p.Ala1853= | |
| XM_011532809.1:c.5559A>T | XP_011531111.1:p.Ala1853= | |
| NM_000384.3:c.5559A>T MANE Select | NP_000375.3:p.Ala1853= |