HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186205223A= , CM000666.2:g.186205223A= | GRCh38 |
NC_000004.11:g.187126377A= , CM000666.1:g.187126377A= | GRCh37 |
NC_000004.10:g.187363371A= | NCBI36 |
NG_007965.1:g.18704A= | |
NG_012095.2:g.1245A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378802.5:c.1011A= MANE Select | ENSP00000368079.4:p.Ala337= | |
ENST00000378802.4:c.1011A= | ENSP00000368079.4:p.Ala337= | |
ENST00000502665.1:n.246A= | ||
ENST00000507209.5:n.5709A= | ||
ENST00000513354.5:n.101A= | ||
NM_207352.3:c.1011A= | NP_997235.3:p.Ala337= | |
XM_005262935.2:c.1011A= | XP_005262992.1:p.Ala337= | |
XM_006714184.2:c.615A= | XP_006714247.1:p.Ala205= | |
XM_005262935.4:c.1011A= | XP_005262992.1:p.Ala337= | |
XM_017008037.1:c.615A= | XP_016863526.1:p.Ala205= | |
NM_207352.4:c.1011A= MANE Select | NP_997235.3:p.Ala337= |