HGVS | Genome Assembly |
---|---|
NC_000001.11:g.9348817C>T , CM000663.2:g.9348817C>T | GRCh38 |
NC_000001.10:g.9408876C>T , CM000663.1:g.9408876C>T | GRCh37 |
NC_000001.9:g.9331463C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000328089.11:c.-149-6926C>T MANE Select | ENSP00000330221.6:n.-149-6926C>T | |
ENST00000328089.10:c.-149-6926C>T | ENSP00000330221.6:n.-149-6926C>T | |
ENST00000450402.1:c.-149-6926C>T | ENSP00000409235.1:n.-149-6926C>T | |
NM_025106.3:c.-149-6926C>T | NP_079382.2:n.-149-6926C>T | |
NM_025106.4:c.-149-6926C>T MANE Select | NP_079382.2:n.-149-6926C>T |