HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190398T>C , CM000663.2:g.204190398T>C | GRCh38 |
NC_000001.10:g.204159526T>C , CM000663.1:g.204159526T>C | GRCh37 |
NC_000001.9:g.202426149T>C | NCBI36 |
NG_032151.1:g.11094A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*86A>G MANE Select | ENSP00000356162.4:n.*86A>G | |
ENST00000367194.4:c.*86A>G | ENSP00000356162.4:n.*86A>G | |
NM_002256.3:c.*86A>G | NP_002247.3:n.*86A>G | |
XM_011509525.1:c.*86A>G | XP_011507827.1:n.*86A>G | |
NM_002256.4:c.*86A>G MANE Select | NP_002247.3:n.*86A>G |