Canonical Allele Identifier: CA884131269

Gene: C3

Linked Data

• dbSNP Id: rs1050240743
• MyVariant Identifiers: chr19:g.6684922C>A (hg19) ; chr19:g.6684911C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6684911C>A , CM000681.2:g.6684911C>A	GRCh38
NC_000019.9:g.6684922C>A , CM000681.1:g.6684922C>A	GRCh37
NC_000019.8:g.6635922C>A	NCBI36
NG_009557.1:g.40741G>T , LRG_27:g.40741G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2318-77G>T
ENST00000695653.1:c.1879-77G>T	ENSP00000512084.1:n.1879-77G>T
ENST00000695654.1:c.2995-77G>T	ENSP00000512085.1:n.2995-77G>T
ENST00000695690.1:n.161-77G>T
ENST00000695691.1:n.161-77G>T
ENST00000245907.11:c.3970-77G>T MANE Select	ENSP00000245907.4:n.3970-77G>T
ENST00000245907.10:c.3970-77G>T	ENSP00000245907.4:n.3970-77G>T
ENST00000596238.1:n.413-77G>T
ENST00000596548.1:c.52-77G>T	ENSP00000469744.1:n.52-77G>T
ENST00000601008.1:c.241+1835G>T	ENSP00000471384.1:n.241+1835G>T
NM_000064.3:c.3970-77G>T	NP_000055.2:n.3970-77G>T
NM_000064.4:c.3970-77G>T MANE Select	NP_000055.2:n.3970-77G>T