Canonical Allele Identifier: CA631722466

Gene: C3

Linked Data

• dbSNP Id: rs1431162769
• gnomAD v2: 19-6710047-A-AGG
• gnomAD v3: 19-6710036-A-AGG
• gnomAD v4: 19-6710036-A-AGG
• MyVariant Identifiers: chr19:g.6710047_6710048insGG (hg19) ; chr19:g.6710036_6710037insGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710037_6710038insGG , CM000681.2:g.6710037_6710038insGG	GRCh38
NC_000019.9:g.6710048_6710049insGG , CM000681.1:g.6710048_6710049insGG	GRCh37
NC_000019.8:g.6661048_6661049insGG	NCBI36
NG_009557.1:g.15615_15616insCC , LRG_27:g.15615_15616insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-195_1564-194insCC	ENSP00000512083.1:n.1564-195_1564-194insCC
ENST00000695654.1:c.811-195_811-194insCC	ENSP00000512085.1:n.811-195_811-194insCC
ENST00000695655.1:c.592-159_592-158insCC	ENSP00000512086.1:n.592-159_592-158insCC
ENST00000695692.1:n.1051-195_1051-194insCC
ENST00000245907.11:c.1687-195_1687-194insCC MANE Select	ENSP00000245907.4:n.1687-195_1687-194insCC
ENST00000245907.10:c.1687-195_1687-194insCC	ENSP00000245907.4:n.1687-195_1687-194insCC
ENST00000600763.1:n.320-195_320-194insCC
NM_000064.3:c.1687-195_1687-194insCC	NP_000055.2:n.1687-195_1687-194insCC
NM_000064.4:c.1687-195_1687-194insCC MANE Select	NP_000055.2:n.1687-195_1687-194insCC