Canonical Allele Identifier: CA505120207

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679422A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679411A>G , CM000681.2:g.6679411A>G	GRCh38
NC_000019.9:g.6679422A>G , CM000681.1:g.6679422A>G	GRCh37
NC_000019.8:g.6630422A>G	NCBI36
NG_009557.1:g.46241T>C , LRG_27:g.46241T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.2890T>C
ENST00000695653.1:c.2451T>C	ENSP00000512084.1:p.Ala817=
ENST00000695654.1:c.3567T>C	ENSP00000512085.1:p.Ala1189=
ENST00000695689.1:c.513T>C	ENSP00000512101.1:n.513T>C
ENST00000695690.1:n.1607T>C
ENST00000695691.1:n.1403T>C
ENST00000245907.11:c.4542T>C MANE Select	ENSP00000245907.4:p.Ala1514=
ENST00000245907.10:c.4542T>C	ENSP00000245907.4:p.Ala1514=
ENST00000599668.1:n.137T>C
ENST00000599899.5:n.1501T>C
ENST00000601008.1:c.242-1453T>C	ENSP00000471384.1:n.242-1453T>C
NM_000064.3:c.4542T>C	NP_000055.2:p.Ala1514=
NM_000064.4:c.4542T>C MANE Select	NP_000055.2:p.Ala1514=