Canonical Allele Identifier: CA884143411

Gene: C3

Linked Data

• dbSNP Id: rs1187565044
• MyVariant Identifiers: chr19:g.6701438_6701439insT (hg19) ; chr19:g.6701427_6701428insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6701428dup , CM000681.2:g.6701428dup	GRCh38
NC_000019.9:g.6701439dup , CM000681.1:g.6701439dup	GRCh37
NC_000019.8:g.6652439dup	NCBI36
NG_009557.1:g.24224dup , LRG_27:g.24224dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.788+699dup
ENST00000695652.1:c.2317+699dup	ENSP00000512083.1:n.2317+699dup
ENST00000695653.1:c.349+699dup	ENSP00000512084.1:n.349+699dup
ENST00000695654.1:c.1564+699dup	ENSP00000512085.1:n.1564+699dup
ENST00000695655.1:c.1381+699dup	ENSP00000512086.1:n.1381+699dup
ENST00000695692.1:n.1804+699dup
ENST00000245907.11:c.2440+699dup MANE Select	ENSP00000245907.4:n.2440+699dup
ENST00000245907.10:c.2440+699dup	ENSP00000245907.4:n.2440+699dup
ENST00000602053.1:n.488+699dup
NM_000064.3:c.2440+699dup	NP_000055.2:n.2440+699dup
NM_000064.4:c.2440+699dup MANE Select	NP_000055.2:n.2440+699dup