Canonical Allele Identifier: CA403633810

Gene: C3

Linked Data

• gnomAD v4: 19-6697678-T-C
• MyVariant Identifiers: chr19:g.6697689T>C (hg19) ; chr19:g.6697678T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697678T>C , CM000681.2:g.6697678T>C	GRCh38
NC_000019.9:g.6697689T>C , CM000681.1:g.6697689T>C	GRCh37
NC_000019.8:g.6648689T>C	NCBI36
NG_009557.1:g.27974A>G , LRG_27:g.27974A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.905A>G
ENST00000695652.1:c.2434A>G	ENSP00000512083.1:p.Asn812Asp
ENST00000695653.1:c.466A>G	ENSP00000512084.1:p.Asn156Asp
ENST00000695654.1:c.1681A>G	ENSP00000512085.1:p.Asn561Asp
ENST00000695655.1:c.1498A>G	ENSP00000512086.1:n.1498A>G
ENST00000695692.1:n.1921A>G
ENST00000245907.11:c.2557A>G MANE Select	ENSP00000245907.4:p.Asn853Asp
ENST00000245907.10:c.2557A>G	ENSP00000245907.4:p.Asn853Asp
ENST00000594005.1:n.38A>G
ENST00000602053.1:n.605A>G
NM_000064.3:c.2557A>G	NP_000055.2:p.Asn853Asp
NM_000064.4:c.2557A>G MANE Select	NP_000055.2:p.Asn853Asp