Canonical Allele Identifier: CA884148686

Gene: C3

Linked Data

• dbSNP Id: rs1241916405
• gnomAD v3: 19-6709978-G-GGA
• gnomAD v4: 19-6709978-G-GGA
• MyVariant Identifiers: chr19:g.6709989_6709990insGA (hg19) ; chr19:g.6709978_6709979insGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709989_6709990dup , CM000681.2:g.6709989_6709990dup	GRCh38
NC_000019.9:g.6710000_6710001dup , CM000681.1:g.6710000_6710001dup	GRCh37
NC_000019.8:g.6661000_6661001dup	NCBI36
NG_009557.1:g.15672_15673dup , LRG_27:g.15672_15673dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-138_1564-137dup	ENSP00000512083.1:n.1564-138_1564-137dup
ENST00000695654.1:c.811-138_811-137dup	ENSP00000512085.1:n.811-138_811-137dup
ENST00000695655.1:c.592-102_592-101dup	ENSP00000512086.1:n.592-102_592-101dup
ENST00000695692.1:n.1051-138_1051-137dup
ENST00000245907.11:c.1687-138_1687-137dup MANE Select	ENSP00000245907.4:n.1687-138_1687-137dup
ENST00000245907.10:c.1687-138_1687-137dup	ENSP00000245907.4:n.1687-138_1687-137dup
ENST00000600763.1:n.320-138_320-137dup
NM_000064.3:c.1687-138_1687-137dup	NP_000055.2:n.1687-138_1687-137dup
NM_000064.4:c.1687-138_1687-137dup MANE Select	NP_000055.2:n.1687-138_1687-137dup