HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31270252T= , CM000668.2:g.31270252T= | GRCh38 |
NC_000006.11:g.31238029T= , CM000668.1:g.31238029T= | GRCh37 |
NC_000006.10:g.31346008T= | NCBI36 |
NG_029422.2:g.6880A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.853A= MANE Select | ENSP00000365402.5:p.Met285= | |
ENST00000376228.9:c.853A= | ENSP00000365402.5:p.Met285= | |
ENST00000376237.8:c.*440A= | ENSP00000365412.4:n.*440A= | |
ENST00000383329.7:c.853A= | ENSP00000372819.3:p.Met285= | |
ENST00000415537.1:c.744A= | ||
ENST00000470363.5:n.171A= | ||
ENST00000487245.5:n.1212A= | ||
ENST00000495835.1:n.1042A= | ||
NM_002117.5:c.853A= | NP_002108.4:p.Met285= | |
NM_002117.6:c.853A= MANE Select | NP_002108.4:p.Met285= |