Canonical Allele Identifier: CA403618328

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6685031A>T (hg19) ; chr19:g.6685020A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685020A>T , CM000681.2:g.6685020A>T	GRCh38
NC_000019.9:g.6685031A>T , CM000681.1:g.6685031A>T	GRCh37
NC_000019.8:g.6636031A>T	NCBI36
NG_009557.1:g.40632T>A , LRG_27:g.40632T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2285T>A
ENST00000695653.1:c.1846T>A	ENSP00000512084.1:p.Trp616Arg
ENST00000695654.1:c.2962T>A	ENSP00000512085.1:p.Trp988Arg
ENST00000695690.1:n.128T>A
ENST00000695691.1:n.128T>A
ENST00000245907.11:c.3937T>A MANE Select	ENSP00000245907.4:p.Trp1313Arg
ENST00000245907.10:c.3937T>A	ENSP00000245907.4:p.Trp1313Arg
ENST00000596238.1:n.380T>A
ENST00000596548.1:c.19T>A	ENSP00000469744.1:p.Trp7Arg
ENST00000601008.1:c.241+1726T>A	ENSP00000471384.1:n.241+1726T>A
NM_000064.3:c.3937T>A	NP_000055.2:p.Trp1313Arg
NM_000064.4:c.3937T>A MANE Select	NP_000055.2:p.Trp1313Arg