HGVS | Genome Assembly |
---|---|
NC_000001.11:g.9348807T= , CM000663.2:g.9348807T= | GRCh38 |
NC_000001.10:g.9408866T= , CM000663.1:g.9408866T= | GRCh37 |
NC_000001.9:g.9331453T= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000328089.11:c.-149-6936T= MANE Select | ENSP00000330221.6:n.-149-6936T= | |
ENST00000328089.10:c.-149-6936T= | ENSP00000330221.6:n.-149-6936T= | |
ENST00000450402.1:c.-149-6936T= | ENSP00000409235.1:n.-149-6936T= | |
NM_025106.3:c.-149-6936T= | NP_079382.2:n.-149-6936T= | |
NM_025106.4:c.-149-6936T= MANE Select | NP_079382.2:n.-149-6936T= |