Canonical Allele Identifier: CA505124524

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6698018_6698019insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6698009dup , CM000681.2:g.6698009dup	GRCh38
NC_000019.9:g.6698020dup , CM000681.1:g.6698020dup	GRCh37
NC_000019.8:g.6649020dup	NCBI36
NG_009557.1:g.27644dup , LRG_27:g.27644dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-214dup
ENST00000695652.1:c.2318-214dup	ENSP00000512083.1:n.2318-214dup
ENST00000695653.1:c.350-214dup	ENSP00000512084.1:n.350-214dup
ENST00000695654.1:c.1565-214dup	ENSP00000512085.1:n.1565-214dup
ENST00000695655.1:c.1382-214dup	ENSP00000512086.1:n.1382-214dup
ENST00000695692.1:n.1805-214dup
ENST00000245907.11:c.2441-214dup MANE Select	ENSP00000245907.4:n.2441-214dup
ENST00000245907.10:c.2441-214dup	ENSP00000245907.4:n.2441-214dup
ENST00000602053.1:n.489-214dup
NM_000064.3:c.2441-214dup	NP_000055.2:n.2441-214dup
NM_000064.4:c.2441-214dup MANE Select	NP_000055.2:n.2441-214dup