HGVS | Genome Assembly |
---|---|
NC_000008.11:g.24956693C>A , CM000670.2:g.24956693C>A | GRCh38 |
NC_000008.10:g.24814207C>A , CM000670.1:g.24814207C>A | GRCh37 |
NC_000008.9:g.24870124C>A | NCBI36 |
NG_008492.1:g.4925G>T , LRG_259:g.4925G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000610854.1:c.-178G>T | ENSP00000482169.1:n.-178G>T | |
ENST00000615973.1:n.29G>T | ||
NM_006158.4:c.-178G>T , LRG_259t1:c.-178G>T | NP_006149.2:n.-178G>T |