Canonical Allele Identifier: CA403611953

Gene: C3

Linked Data

• dbSNP Id: rs112746915
• MyVariant Identifiers: chr19:g.6679135C>G (hg19) ; chr19:g.6679124C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679124C>G , CM000681.2:g.6679124C>G	GRCh38
NC_000019.9:g.6679135C>G , CM000681.1:g.6679135C>G	GRCh37
NC_000019.8:g.6630135C>G	NCBI36
NG_009557.1:g.46528G>C , LRG_27:g.46528G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2978+1G>C
ENST00000695653.1:c.2539+1G>C	ENSP00000512084.1:n.2539+1G>C
ENST00000695654.1:c.3655+1G>C	ENSP00000512085.1:n.3655+1G>C
ENST00000695689.1:c.601+1G>C	ENSP00000512101.1:n.601+1G>C
ENST00000695690.1:n.1695+1G>C
ENST00000695691.1:n.1491+1G>C
ENST00000245907.11:c.4630+1G>C MANE Select	ENSP00000245907.4:n.4630+1G>C
ENST00000245907.10:c.4630+1G>C	ENSP00000245907.4:n.4630+1G>C
ENST00000599668.1:n.250+1G>C
ENST00000599899.5:n.1589+1G>C
ENST00000601008.1:c.242-1166G>C	ENSP00000471384.1:n.242-1166G>C
ENST00000602229.1:c.77+1G>C
NM_000064.3:c.4630+1G>C	NP_000055.2:n.4630+1G>C
NM_000064.4:c.4630+1G>C MANE Select	NP_000055.2:n.4630+1G>C