HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190374T>G , CM000663.2:g.204190374T>G | GRCh38 |
NC_000001.10:g.204159502T>G , CM000663.1:g.204159502T>G | GRCh37 |
NC_000001.9:g.202426125T>G | NCBI36 |
NG_032151.1:g.11118A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*110A>C MANE Select | ENSP00000356162.4:n.*110A>C | |
ENST00000367194.4:c.*110A>C | ENSP00000356162.4:n.*110A>C | |
NM_002256.3:c.*110A>C | NP_002247.3:n.*110A>C | |
XM_011509525.1:c.*110A>C | XP_011507827.1:n.*110A>C | |
NM_002256.4:c.*110A>C MANE Select | NP_002247.3:n.*110A>C |