Linked Data
MyVariant Identifiers:
chr9:g.139568279G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136673827G>C , CM000671.2:g.136673827G>C | GRCh38 |
| NC_000009.11:g.139568279G>C , CM000671.1:g.139568279G>C | GRCh37 |
| NC_000009.10:g.138688100G>C | NCBI36 |
| NG_008090.1:g.18633C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371696.7:c.762C>G MANE Select | ENSP00000360761.2:p.Thr254= | |
| ENST00000371694.7:c.666C>G | ENSP00000360759.3:p.Thr222= | |
| ENST00000371696.6:c.762C>G | ENSP00000360761.2:p.Thr254= | |
| ENST00000472820.1:n.690C>G | ||
| ENST00000538402.1:c.762C>G | ENSP00000438919.1:p.Thr254= | |
| NM_001012727.1:c.666C>G | NP_001012745.1:p.Thr222= | |
| NM_006412.3:c.762C>G | NP_006403.2:p.Thr254= | |
| NM_006412.4:c.762C>G MANE Select | NP_006403.2:p.Thr254= | |
| NM_001012727.2:c.666C>G | NP_001012745.1:p.Thr222= |