Canonical Allele Identifier: CA403639629

Gene: C3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1573A>T	ENSP00000512083.1:p.Lys525Ter
ENST00000695654.1:c.820A>T	ENSP00000512085.1:p.Lys274Ter
ENST00000695655.1:c.637A>T	ENSP00000512086.1:n.637A>T
ENST00000695692.1:n.1060A>T
ENST00000245907.11:c.1696A>T MANE Select	ENSP00000245907.4:p.Lys566Ter
ENST00000245907.10:c.1696A>T	ENSP00000245907.4:p.Lys566Ter
ENST00000600763.1:n.329A>T
NM_000064.3:c.1696A>T	NP_000055.2:p.Lys566Ter
NM_000064.4:c.1696A>T MANE Select	NP_000055.2:p.Lys566Ter