Canonical Allele Identifier: CA403612745

Gene: C3

Linked Data

• dbSNP Id: rs757670171
• gnomAD v2: 19-6679455-G-T
• gnomAD v3: 19-6679444-G-T
• gnomAD v4: 19-6679444-G-T
• MyVariant Identifiers: chr19:g.6679455G>T (hg19) ; chr19:g.6679444G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679444G>T , CM000681.2:g.6679444G>T	GRCh38
NC_000019.9:g.6679455G>T , CM000681.1:g.6679455G>T	GRCh37
NC_000019.8:g.6630455G>T	NCBI36
NG_009557.1:g.46208C>A , LRG_27:g.46208C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2857C>A
ENST00000695653.1:c.2418C>A	ENSP00000512084.1:p.Asn806Lys
ENST00000695654.1:c.3534C>A	ENSP00000512085.1:p.Asn1178Lys
ENST00000695689.1:c.480C>A	ENSP00000512101.1:n.480C>A
ENST00000695690.1:n.1574C>A
ENST00000695691.1:n.1370C>A
ENST00000245907.11:c.4509C>A MANE Select	ENSP00000245907.4:p.Asn1503Lys
ENST00000245907.10:c.4509C>A	ENSP00000245907.4:p.Asn1503Lys
ENST00000599668.1:n.104C>A
ENST00000599899.5:n.1468C>A
ENST00000601008.1:c.242-1486C>A	ENSP00000471384.1:n.242-1486C>A
NM_000064.3:c.4509C>A	NP_000055.2:p.Asn1503Lys
NM_000064.4:c.4509C>A MANE Select	NP_000055.2:p.Asn1503Lys