HGVS | Genome Assembly |
---|---|
NC_000008.11:g.118111523A= , CM000670.2:g.118111523A= | GRCh38 |
NC_000008.10:g.119123762A= , CM000670.1:g.119123762A= | GRCh37 |
NC_000008.9:g.119192943A= | NCBI36 |
NG_007455.2:g.5297T= , LRG_493:g.5297T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378204.7:c.-477T= MANE Select | ENSP00000367446.3:n.-477T= | |
ENST00000378204.6:c.-477T= | ENSP00000367446.2:n.-477T= | |
NM_000127.2:c.-477T= , LRG_493t1:c.-477T= | NP_000118.2:n.-477T= | |
NM_000127.3:c.-477T= MANE Select | NP_000118.2:n.-477T= |