Canonical Allele Identifier: CA9128657

Gene: C3

Linked Data

• ClinVar Variation Id: 741582
• ClinVar RCV Id: RCV000917754 ; RCV002487992
• dbSNP Id: rs754607975
• ExAC: 19:6686243 G / A
• gnomAD v2: 19-6686243-G-A
• gnomAD v3: 19-6686232-G-A
• gnomAD v4: 19-6686232-G-A
• MyVariant Identifiers: chr19:g.6686243G>A (hg19) ; chr19:g.6686232G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686232G>A , CM000681.2:g.6686232G>A	GRCh38
NC_000019.9:g.6686243G>A , CM000681.1:g.6686243G>A	GRCh37
NC_000019.8:g.6637243G>A	NCBI36
NG_009557.1:g.39420C>T , LRG_27:g.39420C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2050C>T
ENST00000695652.1:c.3579C>T	ENSP00000512083.1:p.Ser1193=
ENST00000695653.1:c.1611C>T	ENSP00000512084.1:p.Ser537=
ENST00000695654.1:c.2727C>T	ENSP00000512085.1:p.Ser909=
ENST00000695655.1:c.2643C>T	ENSP00000512086.1:n.2643C>T
ENST00000695692.1:n.3066C>T
ENST00000245907.11:c.3702C>T MANE Select	ENSP00000245907.4:p.Ser1234=
ENST00000245907.10:c.3702C>T	ENSP00000245907.4:p.Ser1234=
ENST00000596238.1:n.145C>T
ENST00000601008.1:c.241+514C>T	ENSP00000471384.1:n.241+514C>T
NM_000064.3:c.3702C>T	NP_000055.2:p.Ser1234=
NM_000064.4:c.3702C>T MANE Select	NP_000055.2:p.Ser1234=