HGVS | Genome Assembly |
---|---|
NC_000006.12:g.35798433C>T , CM000668.2:g.35798433C>T | GRCh38 |
NC_000006.11:g.35766210C>T , CM000668.1:g.35766210C>T | GRCh37 |
NC_000006.10:g.35874188C>T | NCBI36 |
NG_012184.3:g.6228C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651132.1:c.-255+974C>T | ENSP00000498322.1:n.-255+974C>T | |
XM_011514403.1:c.-135+974C>T | XP_011512705.1:n.-135+974C>T |