Canonical Allele Identifier: CA631664632

Gene: C3

Linked Data

• dbSNP Id: rs1483921019
• gnomAD v2: 19-6722602-A-G
• gnomAD v3: 19-6722591-A-G
• gnomAD v4: 19-6722591-A-G
• MyVariant Identifiers: chr19:g.6722602A>G (hg19) ; chr19:g.6722591A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6722591A>G , CM000681.2:g.6722591A>G	GRCh38
NC_000019.9:g.6722602A>G , CM000681.1:g.6722602A>G	GRCh37
NC_000019.8:g.6673602A>G	NCBI36
NG_009557.1:g.3061T>C , LRG_27:g.3061T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000600744.1:c.-50+850T>C	ENSP00000472044.1:n.-50+850T>C