Canonical Allele Identifier: CA505192317

Gene: C3

Linked Data

• dbSNP Id: rs138884408
• MyVariant Identifiers: chr19:g.6697466G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697455G>C , CM000681.2:g.6697455G>C	GRCh38
NC_000019.9:g.6697466G>C , CM000681.1:g.6697466G>C	GRCh37
NC_000019.8:g.6648466G>C	NCBI36
NG_009557.1:g.28197C>G , LRG_27:g.28197C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1033C>G
ENST00000695652.1:c.2562C>G	ENSP00000512083.1:p.Ser854=
ENST00000695653.1:c.594C>G	ENSP00000512084.1:p.Ser198=
ENST00000695654.1:c.1809C>G	ENSP00000512085.1:p.Ser603=
ENST00000695655.1:c.1626C>G	ENSP00000512086.1:n.1626C>G
ENST00000695692.1:n.2049C>G
ENST00000245907.11:c.2685C>G MANE Select	ENSP00000245907.4:p.Ser895=
ENST00000245907.10:c.2685C>G	ENSP00000245907.4:p.Ser895=
ENST00000594005.1:n.261C>G
NM_000064.3:c.2685C>G	NP_000055.2:p.Ser895=
NM_000064.4:c.2685C>G MANE Select	NP_000055.2:p.Ser895=