Canonical Allele Identifier: CA403632699

Gene: C3

Linked Data

• gnomAD v4: 19-6697387-T-C
• MyVariant Identifiers: chr19:g.6697398T>C (hg19) ; chr19:g.6697387T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697387T>C , CM000681.2:g.6697387T>C	GRCh38
NC_000019.9:g.6697398T>C , CM000681.1:g.6697398T>C	GRCh37
NC_000019.8:g.6648398T>C	NCBI36
NG_009557.1:g.28265A>G , LRG_27:g.28265A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1101A>G
ENST00000695652.1:c.2630A>G	ENSP00000512083.1:p.His877Arg
ENST00000695653.1:c.662A>G	ENSP00000512084.1:p.His221Arg
ENST00000695654.1:c.1877A>G	ENSP00000512085.1:p.His626Arg
ENST00000695655.1:c.1694A>G	ENSP00000512086.1:n.1694A>G
ENST00000695692.1:n.2117A>G
ENST00000245907.11:c.2753A>G MANE Select	ENSP00000245907.4:p.His918Arg
ENST00000245907.10:c.2753A>G	ENSP00000245907.4:p.His918Arg
ENST00000594005.1:n.329A>G
NM_000064.3:c.2753A>G	NP_000055.2:p.His918Arg
NM_000064.4:c.2753A>G MANE Select	NP_000055.2:p.His918Arg