HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190382T>G , CM000663.2:g.204190382T>G | GRCh38 |
NC_000001.10:g.204159510T>G , CM000663.1:g.204159510T>G | GRCh37 |
NC_000001.9:g.202426133T>G | NCBI36 |
NG_032151.1:g.11110A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*102A>C MANE Select | ENSP00000356162.4:n.*102A>C | |
ENST00000367194.4:c.*102A>C | ENSP00000356162.4:n.*102A>C | |
NM_002256.3:c.*102A>C | NP_002247.3:n.*102A>C | |
XM_011509525.1:c.*102A>C | XP_011507827.1:n.*102A>C | |
NM_002256.4:c.*102A>C MANE Select | NP_002247.3:n.*102A>C |