Linked Data
MyVariant Identifiers:
chr3:g.119132909C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119414062C>T , CM000665.2:g.119414062C>T | GRCh38 |
| NC_000003.11:g.119132909C>T , CM000665.1:g.119132909C>T | GRCh37 |
| NC_000003.10:g.120615599C>T | NCBI36 |
| NG_007665.2:g.124690C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.2133C>T MANE Select | ENSP00000264245.4:p.Val711= | |
| ENST00000264245.8:c.2133C>T | ENSP00000264245.4:p.Val711= | |
| NM_020754.3:c.2133C>T | NP_065805.2:p.Val711= | |
| XM_005247671.3:c.2040C>T | XP_005247728.1:p.Val680= | |
| XM_006713714.2:c.2073C>T | XP_006713777.1:p.Val691= | |
| XM_006713714.3:c.2073C>T | XP_006713777.1:p.Val691= | |
| XM_017006955.1:c.1641C>T | XP_016862444.1:p.Val547= | |
| NM_020754.4:c.2133C>T MANE Select | NP_065805.2:p.Val711= |