HGVS | Genome Assembly |
---|---|
NC_000008.11:g.118111428T= , CM000670.2:g.118111428T= | GRCh38 |
NC_000008.10:g.119123667T= , CM000670.1:g.119123667T= | GRCh37 |
NC_000008.9:g.119192848T= | NCBI36 |
NG_007455.2:g.5392A= , LRG_493:g.5392A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378204.7:c.-382A= MANE Select | ENSP00000367446.3:n.-382A= | |
ENST00000378204.6:c.-382A= | ENSP00000367446.2:n.-382A= | |
NM_000127.2:c.-382A= , LRG_493t1:c.-382A= | NP_000118.2:n.-382A= | |
NM_000127.3:c.-382A= MANE Select | NP_000118.2:n.-382A= |