Canonical Allele Identifier: CA505192374

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697547G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697536G>A , CM000681.2:g.6697536G>A	GRCh38
NC_000019.9:g.6697547G>A , CM000681.1:g.6697547G>A	GRCh37
NC_000019.8:g.6648547G>A	NCBI36
NG_009557.1:g.28116C>T , LRG_27:g.28116C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.952C>T
ENST00000695652.1:c.2481C>T	ENSP00000512083.1:p.His827=
ENST00000695653.1:c.513C>T	ENSP00000512084.1:p.His171=
ENST00000695654.1:c.1728C>T	ENSP00000512085.1:p.His576=
ENST00000695655.1:c.1545C>T	ENSP00000512086.1:n.1545C>T
ENST00000695692.1:n.1968C>T
ENST00000245907.11:c.2604C>T MANE Select	ENSP00000245907.4:p.His868=
ENST00000245907.10:c.2604C>T	ENSP00000245907.4:p.His868=
ENST00000594005.1:n.180C>T
NM_000064.3:c.2604C>T	NP_000055.2:p.His868=
NM_000064.4:c.2604C>T MANE Select	NP_000055.2:p.His868=