HGVS | Genome Assembly |
---|---|
NC_000022.11:g.37710220A= , CM000684.2:g.37710220A= | GRCh38 |
NC_000022.10:g.38106227A= , CM000684.1:g.38106227A= | GRCh37 |
NC_000022.9:g.36436173A= | NCBI36 |
NG_012857.1:g.18233A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644935.1:c.115-207A= MANE Select | ENSP00000496394.1:n.115-207A= | |
ENST00000344404.10:c.115-207A= | ENSP00000340312.6:n.115-207A= | |
ENST00000406386.7:c.115-207A= | ENSP00000384312.3:n.115-207A= | |
ENST00000455236.4:c.1072-207A= | ENSP00000477208.1:n.1072-207A= | |
ENST00000492485.5:n.251-207A= | ||
NM_001039141.2:c.115-207A= | NP_001034230.1:n.115-207A= | |
NM_001039141.3:c.115-207A= MANE Select | NP_001034230.1:n.115-207A= |