Canonical Allele Identifier: CA403612821

Gene: C3

Linked Data

• dbSNP Id: rs368362113
• gnomAD v4: 19-6679469-G-C
• MyVariant Identifiers: chr19:g.6679480G>C (hg19) ; chr19:g.6679469G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679469G>C , CM000681.2:g.6679469G>C	GRCh38
NC_000019.9:g.6679480G>C , CM000681.1:g.6679480G>C	GRCh37
NC_000019.8:g.6630480G>C	NCBI36
NG_009557.1:g.46183C>G , LRG_27:g.46183C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2832C>G
ENST00000695653.1:c.2393C>G	ENSP00000512084.1:p.Pro798Arg
ENST00000695654.1:c.3509C>G	ENSP00000512085.1:p.Pro1170Arg
ENST00000695689.1:c.455C>G	ENSP00000512101.1:n.455C>G
ENST00000695690.1:n.1549C>G
ENST00000695691.1:n.1345C>G
ENST00000245907.11:c.4484C>G MANE Select	ENSP00000245907.4:p.Pro1495Arg
ENST00000245907.10:c.4484C>G	ENSP00000245907.4:p.Pro1495Arg
ENST00000599668.1:n.79C>G
ENST00000599899.5:n.1443C>G
ENST00000601008.1:c.242-1511C>G	ENSP00000471384.1:n.242-1511C>G
NM_000064.3:c.4484C>G	NP_000055.2:p.Pro1495Arg
NM_000064.4:c.4484C>G MANE Select	NP_000055.2:p.Pro1495Arg