Canonical Allele Identifier: CA403615525

Gene: C3

Linked Data

• gnomAD v4: 19-6682213-C-T
• MyVariant Identifiers: chr19:g.6682224C>T (hg19) ; chr19:g.6682213C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682213C>T , CM000681.2:g.6682213C>T	GRCh38
NC_000019.9:g.6682224C>T , CM000681.1:g.6682224C>T	GRCh37
NC_000019.8:g.6633224C>T	NCBI36
NG_009557.1:g.43439G>A , LRG_27:g.43439G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2537G>A
ENST00000695653.1:c.2098G>A	ENSP00000512084.1:p.Asp700Asn
ENST00000695654.1:c.3214G>A	ENSP00000512085.1:p.Asp1072Asn
ENST00000695689.1:c.160G>A	ENSP00000512101.1:n.160G>A
ENST00000695690.1:n.380G>A
ENST00000695691.1:n.380G>A
ENST00000245907.11:c.4189G>A MANE Select	ENSP00000245907.4:p.Asp1397Asn
ENST00000245907.10:c.4189G>A	ENSP00000245907.4:p.Asp1397Asn
ENST00000596548.1:c.310G>A	ENSP00000469744.1:p.Asp104Asn
ENST00000599899.5:n.1148G>A
ENST00000601008.1:c.242-4255G>A	ENSP00000471384.1:n.242-4255G>A
NM_000064.3:c.4189G>A	NP_000055.2:p.Asp1397Asn
NM_000064.4:c.4189G>A MANE Select	NP_000055.2:p.Asp1397Asn