HGVS | Genome Assembly |
---|---|
NC_000019.10:g.1399816A>C , CM000681.2:g.1399816A>C | GRCh38 |
NC_000019.9:g.1399815A>C , CM000681.1:g.1399815A>C | GRCh37 |
NC_000019.8:g.1350815A>C | NCBI36 |
NG_009785.1:g.6738T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252288.8:c.304T>G MANE Select | ENSP00000252288.1:p.Trp102Gly | |
ENST00000447102.8:c.304T>G | ENSP00000403536.2:p.Trp102Gly | |
ENST00000640762.1:c.235T>G | ENSP00000492031.1:p.Trp79Gly | |
ENST00000252288.6:c.304T>G | ENSP00000252288.1:p.Trp102Gly | |
ENST00000447102.7:c.304T>G | ENSP00000403536.2:p.Trp102Gly | |
NM_000156.5:c.304T>G | NP_000147.1:p.Trp102Gly | |
NM_138924.2:c.304T>G | NP_620279.1:p.Trp102Gly | |
NM_000156.6:c.304T>G MANE Select | NP_000147.1:p.Trp102Gly | |
NM_138924.3:c.304T>G | NP_620279.1:p.Trp102Gly |