HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18783131A= , CM000681.2:g.18783131A= | GRCh38 |
NC_000019.9:g.18893941A= , CM000681.1:g.18893941A= | GRCh37 |
NC_000019.8:g.18754941A= | NCBI36 |
NG_007070.1:g.13174T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222271.7:c.2150T= MANE Select | ENSP00000222271.2:p.Met717= | |
ENST00000222271.6:c.2150T= | ENSP00000222271.2:p.Met717= | |
ENST00000425807.1:c.1991T= | ENSP00000403792.1:p.Met664= | |
ENST00000542601.6:c.2051T= | ENSP00000439156.2:p.Met684= | |
NM_000095.2:c.2150T= | NP_000086.2:p.Met717= | |
NM_000095.3:c.2150T= MANE Select | NP_000086.2:p.Met717= |