Canonical Allele Identifier: CA403643221

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6714232G>T (hg19) ; chr19:g.6714221G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714221G>T , CM000681.2:g.6714221G>T	GRCh38
NC_000019.9:g.6714232G>T , CM000681.1:g.6714232G>T	GRCh37
NC_000019.8:g.6665232G>T	NCBI36
NG_009557.1:g.11431C>A , LRG_27:g.11431C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.504C>A	ENSP00000512083.1:p.Tyr168Ter
ENST00000245907.11:c.627C>A MANE Select	ENSP00000245907.4:p.Tyr209Ter
ENST00000245907.10:c.627C>A	ENSP00000245907.4:p.Tyr209Ter
ENST00000595577.1:n.131C>A
NM_000064.3:c.627C>A	NP_000055.2:p.Tyr209Ter
NM_000064.4:c.627C>A MANE Select	NP_000055.2:p.Tyr209Ter