Canonical Allele Identifier: CA403632685

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697395T>G (hg19) ; chr19:g.6697384T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697384T>G , CM000681.2:g.6697384T>G	GRCh38
NC_000019.9:g.6697395T>G , CM000681.1:g.6697395T>G	GRCh37
NC_000019.8:g.6648395T>G	NCBI36
NG_009557.1:g.28268A>C , LRG_27:g.28268A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1104A>C
ENST00000695652.1:c.2633A>C	ENSP00000512083.1:p.His878Pro
ENST00000695653.1:c.665A>C	ENSP00000512084.1:p.His222Pro
ENST00000695654.1:c.1880A>C	ENSP00000512085.1:p.His627Pro
ENST00000695655.1:c.1697A>C	ENSP00000512086.1:n.1697A>C
ENST00000695692.1:n.2120A>C
ENST00000245907.11:c.2756A>C MANE Select	ENSP00000245907.4:p.His919Pro
ENST00000245907.10:c.2756A>C	ENSP00000245907.4:p.His919Pro
ENST00000594005.1:n.332A>C
NM_000064.3:c.2756A>C	NP_000055.2:p.His919Pro
NM_000064.4:c.2756A>C MANE Select	NP_000055.2:p.His919Pro