HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135299T>G , CM000664.2:g.26135299T>G | GRCh38 |
NC_000002.11:g.26358168T>G , CM000664.1:g.26358168T>G | GRCh37 |
NC_000002.10:g.26211672T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264710.5:c.*278T>G MANE Select | ENSP00000264710.4:n.*278T>G | |
ENST00000264710.4:c.*278T>G | ENSP00000264710.4:n.*278T>G | |
ENST00000495146.5:n.1244T>G | ||
NM_016131.4:c.*278T>G | NP_057215.3:n.*278T>G | |
XM_024452565.1:c.*278T>G | XP_024308333.1:n.*278T>G | |
NM_016131.5:c.*278T>G MANE Select | NP_057215.3:n.*278T>G |