Canonical Allele Identifier: CA884137303

Gene: C3

Linked Data

• dbSNP Id: rs1181420378
• gnomAD v3: 19-6722590-G-A
• gnomAD v4: 19-6722590-G-A
• MyVariant Identifiers: chr19:g.6722601G>A (hg19) ; chr19:g.6722590G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6722590G>A , CM000681.2:g.6722590G>A	GRCh38
NC_000019.9:g.6722601G>A , CM000681.1:g.6722601G>A	GRCh37
NC_000019.8:g.6673601G>A	NCBI36
NG_009557.1:g.3062C>T , LRG_27:g.3062C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000600744.1:c.-50+851C>T	ENSP00000472044.1:n.-50+851C>T