HGVS | Genome Assembly |
---|---|
NC_000006.12:g.35797903G>T , CM000668.2:g.35797903G>T | GRCh38 |
NC_000006.11:g.35765680G>T , CM000668.1:g.35765680G>T | GRCh37 |
NC_000006.10:g.35873658G>T | NCBI36 |
NG_012184.3:g.5698G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651132.1:c.-255+444G>T | ENSP00000498322.1:n.-255+444G>T | |
XM_011514403.1:c.-135+444G>T | XP_011512705.1:n.-135+444G>T |