Canonical Allele Identifier: CA505124836

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6709851C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709840C>A , CM000681.2:g.6709840C>A	GRCh38
NC_000019.9:g.6709851C>A , CM000681.1:g.6709851C>A	GRCh37
NC_000019.8:g.6660851C>A	NCBI36
NG_009557.1:g.15812G>T , LRG_27:g.15812G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1566G>T	ENSP00000512083.1:p.Leu522=
ENST00000695654.1:c.813G>T	ENSP00000512085.1:p.Leu271=
ENST00000695655.1:c.630G>T	ENSP00000512086.1:n.630G>T
ENST00000695692.1:n.1053G>T
ENST00000245907.11:c.1689G>T MANE Select	ENSP00000245907.4:p.Leu563=
ENST00000245907.10:c.1689G>T	ENSP00000245907.4:p.Leu563=
ENST00000600763.1:n.322G>T
NM_000064.3:c.1689G>T	NP_000055.2:p.Leu563=
NM_000064.4:c.1689G>T MANE Select	NP_000055.2:p.Leu563=