Canonical Allele Identifier: CA403618697

Gene: C3

Linked Data

• dbSNP Id: rs757158061
• MyVariant Identifiers: chr19:g.6685157C>A (hg19) ; chr19:g.6685146C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685146C>A , CM000681.2:g.6685146C>A	GRCh38
NC_000019.9:g.6685157C>A , CM000681.1:g.6685157C>A	GRCh37
NC_000019.8:g.6636157C>A	NCBI36
NG_009557.1:g.40506G>T , LRG_27:g.40506G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2159G>T
ENST00000695653.1:c.1720G>T	ENSP00000512084.1:p.Ala574Ser
ENST00000695654.1:c.2836G>T	ENSP00000512085.1:p.Ala946Ser
ENST00000695690.1:n.2G>T
ENST00000695691.1:n.2G>T
ENST00000245907.11:c.3811G>T MANE Select	ENSP00000245907.4:p.Ala1271Ser
ENST00000245907.10:c.3811G>T	ENSP00000245907.4:p.Ala1271Ser
ENST00000596238.1:n.254G>T
ENST00000601008.1:c.241+1600G>T	ENSP00000471384.1:n.241+1600G>T
NM_000064.3:c.3811G>T	NP_000055.2:p.Ala1271Ser
NM_000064.4:c.3811G>T MANE Select	NP_000055.2:p.Ala1271Ser