Linked Data
MyVariant Identifiers:
chr2:g.183703331A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.182838603A>T , CM000664.2:g.182838603A>T | GRCh38 |
| NC_000002.11:g.183703331A>T , CM000664.1:g.183703331A>T | GRCh37 |
| NC_000002.10:g.183411576A>T | NCBI36 |
| NG_017197.1:g.33168T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295113.5:c.603T>A MANE Select | ENSP00000295113.4:p.Ala201= | |
| ENST00000295113.4:c.603T>A | ENSP00000295113.4:p.Ala201= | |
| NM_001463.3:c.603T>A | NP_001454.2:p.Ala201= | |
| NM_001463.4:c.603T>A MANE Select | NP_001454.2:p.Ala201= |