Canonical Allele Identifier: CA2320550414
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6679425G= , CM000681.2:g.6679425G= GRCh38
NC_000019.9:g.6679436G= , CM000681.1:g.6679436G= GRCh37
NC_000019.8:g.6630436G= NCBI36
NG_009557.1:g.46227C= , LRG_27:g.46227C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.2876C=
ENST00000695653.1:c.2437C= ENSP00000512084.1:p.Leu813=
ENST00000695654.1:c.3553C= ENSP00000512085.1:p.Leu1185=
ENST00000695689.1:c.499C= ENSP00000512101.1:n.499C=
ENST00000695690.1:n.1593C=
ENST00000695691.1:n.1389C=
ENST00000245907.11:c.4528C= MANE Select ENSP00000245907.4:p.Leu1510=
ENST00000245907.10:c.4528C= ENSP00000245907.4:p.Leu1510=
ENST00000599668.1:n.123C=
ENST00000599899.5:n.1487C=
ENST00000601008.1:c.242-1467C= ENSP00000471384.1:n.242-1467C=
NM_000064.3:c.4528C= NP_000055.2:p.Leu1510=
NM_000064.4:c.4528C= MANE Select NP_000055.2:p.Leu1510=