Canonical Allele Identifier: CA403643567

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6714433G>A (hg19) ; chr19:g.6714422G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714422G>A , CM000681.2:g.6714422G>A	GRCh38
NC_000019.9:g.6714433G>A , CM000681.1:g.6714433G>A	GRCh37
NC_000019.8:g.6665433G>A	NCBI36
NG_009557.1:g.11230C>T , LRG_27:g.11230C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.406C>T	ENSP00000512083.1:p.Gln136Ter
ENST00000245907.11:c.529C>T MANE Select	ENSP00000245907.4:p.Gln177Ter
ENST00000245907.10:c.529C>T	ENSP00000245907.4:p.Gln177Ter
NM_000064.3:c.529C>T	NP_000055.2:p.Gln177Ter
NM_000064.4:c.529C>T MANE Select	NP_000055.2:p.Gln177Ter