HGVS | Genome Assembly |
---|---|
NC_000009.12:g.136676605A>C , CM000671.2:g.136676605A>C | GRCh38 |
NC_000009.11:g.139571057A>C , CM000671.1:g.139571057A>C | GRCh37 |
NC_000009.10:g.138690878A>C | NCBI36 |
NG_008090.1:g.15855T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371696.7:c.568T>G MANE Select | ENSP00000360761.2:p.Tyr190Asp | |
ENST00000371694.7:c.492+356T>G | ENSP00000360759.3:n.492+356T>G | |
ENST00000371696.6:c.568T>G | ENSP00000360761.2:p.Tyr190Asp | |
ENST00000472820.1:n.496T>G | ||
ENST00000538402.1:c.568T>G | ENSP00000438919.1:p.Tyr190Asp | |
NM_001012727.1:c.492+356T>G | NP_001012745.1:n.492+356T>G | |
NM_006412.3:c.568T>G | NP_006403.2:p.Tyr190Asp | |
NM_006412.4:c.568T>G MANE Select | NP_006403.2:p.Tyr190Asp | |
NM_001012727.2:c.492+356T>G | NP_001012745.1:n.492+356T>G |