HGVS | Genome Assembly |
---|---|
NC_000020.11:g.35438297C>T , CM000682.2:g.35438297C>T | GRCh38 |
NC_000020.10:g.34026077C>T , CM000682.1:g.34026077C>T | GRCh37 |
NC_000020.9:g.33489491C>T | NCBI36 |
NG_008076.2:g.4923G>A | |
NG_008076.3:g.21450G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000374372.1:c.-241-128G>A | ENSP00000363492.1:n.-241-128G>A | |
XM_011529075.1:c.-241-128G>A | XP_011527377.1:n.-241-128G>A | |
XM_011529076.1:c.-241-128G>A | XP_011527378.1:n.-241-128G>A | |
NM_001319138.1:c.-241-128G>A | NP_001306067.1:n.-241-128G>A | |
NM_001319138.2:c.-241-128G>A | NP_001306067.1:n.-241-128G>A |