Canonical Allele Identifier: CA403612767

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679459A>G (hg19) ; chr19:g.6679448A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679448A>G , CM000681.2:g.6679448A>G	GRCh38
NC_000019.9:g.6679459A>G , CM000681.1:g.6679459A>G	GRCh37
NC_000019.8:g.6630459A>G	NCBI36
NG_009557.1:g.46204T>C , LRG_27:g.46204T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2853T>C
ENST00000695653.1:c.2414T>C	ENSP00000512084.1:p.Leu805Pro
ENST00000695654.1:c.3530T>C	ENSP00000512085.1:p.Leu1177Pro
ENST00000695689.1:c.476T>C	ENSP00000512101.1:n.476T>C
ENST00000695690.1:n.1570T>C
ENST00000695691.1:n.1366T>C
ENST00000245907.11:c.4505T>C MANE Select	ENSP00000245907.4:p.Leu1502Pro
ENST00000245907.10:c.4505T>C	ENSP00000245907.4:p.Leu1502Pro
ENST00000599668.1:n.100T>C
ENST00000599899.5:n.1464T>C
ENST00000601008.1:c.242-1490T>C	ENSP00000471384.1:n.242-1490T>C
NM_000064.3:c.4505T>C	NP_000055.2:p.Leu1502Pro
NM_000064.4:c.4505T>C MANE Select	NP_000055.2:p.Leu1502Pro