HGVS | Genome Assembly |
---|---|
NC_000013.11:g.28355514T= , CM000675.2:g.28355514T= | GRCh38 |
NC_000013.10:g.28929651T= , CM000675.1:g.28929651T= | GRCh37 |
NC_000013.9:g.27827651T= | NCBI36 |
NG_012003.1:g.144615A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282397.9:c.2248+2040A= MANE Select | ENSP00000282397.4:n.2248+2040A= | |
ENST00000282397.8:c.2248+2040A= | ENSP00000282397.4:n.2248+2040A= | |
NM_002019.4:c.2248+2040A= MANE Select | NP_002010.2:n.2248+2040A= | |
XM_017020485.1:c.2248+2040A= | XP_016875974.1:n.2248+2040A= |