HGVS | Genome Assembly |
---|---|
NC_000002.12:g.85581777C>T , CM000664.2:g.85581777C>T | GRCh38 |
NC_000002.11:g.85808900C>T , CM000664.1:g.85808900C>T | GRCh37 |
NC_000002.10:g.85662411C>T | NCBI36 |
NG_022887.1:g.9287C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263864.10:c.*61C>T MANE Select | ENSP00000263864.5:n.*61C>T | |
ENST00000263864.9:c.*61C>T | ENSP00000263864.5:n.*61C>T | |
ENST00000409760.1:c.*197C>T | ENSP00000387094.1:n.*197C>T | |
ENST00000432071.1:c.*61C>T | ENSP00000407984.1:n.*61C>T | |
NM_003761.4:c.*61C>T | NP_003752.2:n.*61C>T | |
XM_017005170.1:c.*197C>T | XP_016860659.1:n.*197C>T | |
NM_003761.5:c.*61C>T MANE Select | NP_003752.2:n.*61C>T |