Canonical Allele Identifier: CA884137275
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1337556952
gnomAD v3: 19-6722476-A-C
gnomAD v4: 19-6722476-A-C
MyVariant Identifiers: chr19:g.6722487A>C (hg19) chr19:g.6722476A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722476A>C , CM000681.2:g.6722476A>C GRCh38
NC_000019.9:g.6722487A>C , CM000681.1:g.6722487A>C GRCh37
NC_000019.8:g.6673487A>C NCBI36
NG_009557.1:g.3176T>G , LRG_27:g.3176T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000600744.1:c.-50+965T>G ENSP00000472044.1:n.-50+965T>G
Search 100 bp 5'
Search 100 bp 3'