Canonical Allele Identifier: CA2320567900

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713389G= , CM000681.2:g.6713389G=	GRCh38
NC_000019.9:g.6713400G= , CM000681.1:g.6713400G=	GRCh37
NC_000019.8:g.6664400G=	NCBI36
NG_009557.1:g.12263C= , LRG_27:g.12263C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.753+18C=	ENSP00000512083.1:n.753+18C=
ENST00000695692.1:n.200+18C=
ENST00000245907.11:c.876+18C= MANE Select	ENSP00000245907.4:n.876+18C=
ENST00000245907.10:c.876+18C=	ENSP00000245907.4:n.876+18C=
ENST00000595577.1:n.380+18C=
ENST00000597442.5:n.126+18C=
NM_000064.3:c.876+18C=	NP_000055.2:n.876+18C=
NM_000064.4:c.876+18C= MANE Select	NP_000055.2:n.876+18C=