HGVS | Genome Assembly |
---|---|
NC_000009.12:g.78304857G>T , CM000671.2:g.78304857G>T | GRCh38 |
NC_000009.11:g.80919773G>T , CM000671.1:g.80919773G>T | GRCh37 |
NC_000009.10:g.80109593G>T | NCBI36 |
NG_012165.1:g.12715G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376588.4:c.314G>T MANE Select | ENSP00000365773.3:p.Gly105Val | |
ENST00000347159.6:c.314G>T | ENSP00000317606.2:p.Gly105Val | |
ENST00000376588.3:c.314G>T | ENSP00000365773.3:p.Gly105Val | |
NM_021154.4:c.314G>T | NP_066977.1:p.Gly105Val | |
NM_058179.3:c.314G>T | NP_478059.1:p.Gly105Val | |
NM_058179.4:c.314G>T MANE Select | NP_478059.1:p.Gly105Val | |
NM_021154.5:c.314G>T | NP_066977.1:p.Gly105Val |