Linked Data
MyVariant Identifiers:
chr3:g.138665502A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138946660A>T , CM000665.2:g.138946660A>T | GRCh38 |
| NC_000003.11:g.138665502A>T , CM000665.1:g.138665502A>T | GRCh37 |
| NC_000003.10:g.140148192A>T | NCBI36 |
| NG_012454.1:g.5481T>A | |
| NG_029796.1:g.4427A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648323.1:c.63T>A MANE Select | ENSP00000497217.1:p.Gly21= | |
| ENST00000330315.3:c.63T>A | ENSP00000333188.3:p.Gly21= | |
| NM_023067.3:c.63T>A | NP_075555.1:p.Gly21= | |
| NM_023067.4:c.63T>A MANE Select | NP_075555.1:p.Gly21= |