Canonical Allele Identifier: CA884140897

Gene: C3

Linked Data

• dbSNP Id: rs146892701
• gnomAD v3: 19-6697989-T-TTTATTATTATTA
• gnomAD v4: 19-6697989-T-TTTATTATTATTA
• MyVariant Identifiers: chr19:g.6698000_6698001insTTATTATTATTA (hg19) ; chr19:g.6697989_6697990insTTATTATTATTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6698017_6698028dup , CM000681.2:g.6698017_6698028dup	GRCh38
NC_000019.9:g.6698028_6698039dup , CM000681.1:g.6698028_6698039dup	GRCh37
NC_000019.8:g.6649028_6649039dup	NCBI36
NG_009557.1:g.27651_27662dup , LRG_27:g.27651_27662dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-207_789-196dup
ENST00000695652.1:c.2318-207_2318-196dup	ENSP00000512083.1:n.2318-207_2318-196dup
ENST00000695653.1:c.350-207_350-196dup	ENSP00000512084.1:n.350-207_350-196dup
ENST00000695654.1:c.1565-207_1565-196dup	ENSP00000512085.1:n.1565-207_1565-196dup
ENST00000695655.1:c.1382-207_1382-196dup	ENSP00000512086.1:n.1382-207_1382-196dup
ENST00000695692.1:n.1805-207_1805-196dup
ENST00000245907.11:c.2441-207_2441-196dup MANE Select	ENSP00000245907.4:n.2441-207_2441-196dup
ENST00000245907.10:c.2441-207_2441-196dup	ENSP00000245907.4:n.2441-207_2441-196dup
ENST00000602053.1:n.489-207_489-196dup
NM_000064.3:c.2441-207_2441-196dup	NP_000055.2:n.2441-207_2441-196dup
NM_000064.4:c.2441-207_2441-196dup MANE Select	NP_000055.2:n.2441-207_2441-196dup