HGVS | Genome Assembly |
---|---|
NC_000002.12:g.96143481G= , CM000664.2:g.96143481G= | GRCh38 |
NC_000002.11:g.96809220G= , CM000664.1:g.96809220G= | GRCh37 |
NC_000002.10:g.96172947G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000288943.5:c.*342C= MANE Select | ENSP00000288943.4:n.*342C= | |
ENST00000288943.4:c.*342C= | ENSP00000288943.4:n.*342C= | |
NM_004418.3:c.*342C= | NP_004409.1:n.*342C= | |
XM_017003546.1:c.*342C= | XP_016859035.1:n.*342C= | |
NM_004418.4:c.*342C= MANE Select | NP_004409.1:n.*342C= |