HGVS | Genome Assembly |
---|---|
NC_000008.11:g.24956851C>T , CM000670.2:g.24956851C>T | GRCh38 |
NC_000008.10:g.24814365C>T , CM000670.1:g.24814365C>T | GRCh37 |
NC_000008.9:g.24870282C>T | NCBI36 |
NG_008492.1:g.4767G>A , LRG_259:g.4767G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000610854.1:c.-336G>A | ENSP00000482169.1:n.-336G>A | |
NM_006158.4:c.-336G>A , LRG_259t1:c.-336G>A | NP_006149.2:n.-336G>A |