Canonical Allele Identifier: CA403639632

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6709844T>G (hg19) ; chr19:g.6709833T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709833T>G , CM000681.2:g.6709833T>G	GRCh38
NC_000019.9:g.6709844T>G , CM000681.1:g.6709844T>G	GRCh37
NC_000019.8:g.6660844T>G	NCBI36
NG_009557.1:g.15819A>C , LRG_27:g.15819A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1573A>C	ENSP00000512083.1:p.Lys525Gln
ENST00000695654.1:c.820A>C	ENSP00000512085.1:p.Lys274Gln
ENST00000695655.1:c.637A>C	ENSP00000512086.1:n.637A>C
ENST00000695692.1:n.1060A>C
ENST00000245907.11:c.1696A>C MANE Select	ENSP00000245907.4:p.Lys566Gln
ENST00000245907.10:c.1696A>C	ENSP00000245907.4:p.Lys566Gln
ENST00000600763.1:n.329A>C
NM_000064.3:c.1696A>C	NP_000055.2:p.Lys566Gln
NM_000064.4:c.1696A>C MANE Select	NP_000055.2:p.Lys566Gln