Linked Data
MyVariant Identifiers:
chr3:g.119133161T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119414314T>C , CM000665.2:g.119414314T>C | GRCh38 |
| NC_000003.11:g.119133161T>C , CM000665.1:g.119133161T>C | GRCh37 |
| NC_000003.10:g.120615851T>C | NCBI36 |
| NG_007665.2:g.124942T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.2385T>C MANE Select | ENSP00000264245.4:p.Thr795= | |
| ENST00000264245.8:c.2385T>C | ENSP00000264245.4:p.Thr795= | |
| NM_020754.3:c.2385T>C | NP_065805.2:p.Thr795= | |
| XM_005247671.3:c.2292T>C | XP_005247728.1:p.Thr764= | |
| XM_006713714.2:c.2325T>C | XP_006713777.1:p.Thr775= | |
| XM_006713714.3:c.2325T>C | XP_006713777.1:p.Thr775= | |
| XM_017006955.1:c.1893T>C | XP_016862444.1:p.Thr631= | |
| NM_020754.4:c.2385T>C MANE Select | NP_065805.2:p.Thr795= |