HGVS | Genome Assembly |
---|---|
NC_000011.10:g.101452287C>T , CM000673.2:g.101452287C>T | GRCh38 |
NC_000011.9:g.101323018C>T , CM000673.1:g.101323018C>T | GRCh37 |
NC_000011.8:g.100828228C>T | NCBI36 |
NG_011476.1:g.136642G>A | |
NG_011476.2:g.136642G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344327.8:c.*668G>A MANE Select | ENSP00000340913.3:n.*668G>A | |
ENST00000344327.7:c.*668G>A | ENSP00000340913.3:n.*668G>A | |
NM_004621.5:c.*668G>A | NP_004612.2:n.*668G>A | |
XM_006718898.2:c.*668G>A | XP_006718961.1:n.*668G>A | |
XM_011542968.1:c.*668G>A | XP_011541270.1:n.*668G>A | |
XR_947953.1:n.3179C>T | ||
XM_011542968.3:c.*668G>A | XP_011541270.1:n.*668G>A | |
XM_017018221.2:c.*668G>A | XP_016873710.1:n.*668G>A | |
XR_001747948.2:n.3821G>A | ||
NM_004621.6:c.*668G>A MANE Select | NP_004612.2:n.*668G>A |