HGVS | Genome Assembly |
---|---|
NC_000008.11:g.118111489T= , CM000670.2:g.118111489T= | GRCh38 |
NC_000008.10:g.119123728T= , CM000670.1:g.119123728T= | GRCh37 |
NC_000008.9:g.119192909T= | NCBI36 |
NG_007455.2:g.5331A= , LRG_493:g.5331A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378204.7:c.-443A= MANE Select | ENSP00000367446.3:n.-443A= | |
ENST00000378204.6:c.-443A= | ENSP00000367446.2:n.-443A= | |
NM_000127.2:c.-443A= , LRG_493t1:c.-443A= | NP_000118.2:n.-443A= | |
NM_000127.3:c.-443A= MANE Select | NP_000118.2:n.-443A= |