HGVS | Genome Assembly |
---|---|
NC_000010.11:g.62528623G>T , CM000672.2:g.62528623G>T | GRCh38 |
NC_000010.10:g.64288382G>T , CM000672.1:g.64288382G>T | GRCh37 |
NC_000010.9:g.63958388G>T | NCBI36 |
NG_021209.1:g.159467G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647733.1:c.981+68826G>T | ENSP00000502188.1:n.981+68826G>T | |
ENST00000395251.5:c.-185+8026G>T | ENSP00000378672.1:n.-185+8026G>T | |
ENST00000410046.7:c.981+68826G>T | ENSP00000387091.3:n.981+68826G>T | |
NM_199451.2:c.981+68826G>T | NP_955523.1:n.981+68826G>T | |
NM_199452.3:c.-185+8026G>T | NP_955524.3:n.-185+8026G>T | |
XM_017015937.2:c.982-15586G>T | XP_016871426.1:n.982-15586G>T | |
NM_199451.3:c.981+68826G>T | NP_955523.1:n.981+68826G>T |