HGVS | Genome Assembly |
---|---|
NC_000012.12:g.107001342C>A , CM000674.2:g.107001342C>A | GRCh38 |
NC_000012.11:g.107395120C>A , CM000674.1:g.107395120C>A | GRCh37 |
NC_000012.10:g.105919250C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000008527.10:c.622G>T MANE Select | ENSP00000008527.5:p.Ala208Ser | |
ENST00000008527.9:c.622G>T | ENSP00000008527.5:p.Ala208Ser | |
ENST00000546722.1:n.115G>T | ||
ENST00000552790.5:n.1181G>T | ||
NM_004075.4:c.622G>T | NP_004066.1:p.Ala208Ser | |
XM_011537939.1:c.538G>T | XP_011536241.1:p.Ala180Ser | |
XM_017018832.2:c.538G>T | XP_016874321.1:p.Ala180Ser | |
XM_024448844.1:c.622G>T | XP_024304612.1:p.Ala208Ser | |
XM_024448845.1:c.538G>T | XP_024304613.1:p.Ala180Ser | |
NM_004075.5:c.622G>T MANE Select | NP_004066.1:p.Ala208Ser |