HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190417C>A , CM000663.2:g.204190417C>A | GRCh38 |
NC_000001.10:g.204159545C>A , CM000663.1:g.204159545C>A | GRCh37 |
NC_000001.9:g.202426168C>A | NCBI36 |
NG_032151.1:g.11075G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*67G>T MANE Select | ENSP00000356162.4:n.*67G>T | |
ENST00000367194.4:c.*67G>T | ENSP00000356162.4:n.*67G>T | |
NM_002256.3:c.*67G>T | NP_002247.3:n.*67G>T | |
XM_011509525.1:c.*67G>T | XP_011507827.1:n.*67G>T | |
NM_002256.4:c.*67G>T MANE Select | NP_002247.3:n.*67G>T |