Canonical Allele Identifier: CA993061102
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1968209834
gnomAD v3: 19-6722689-G-C
gnomAD v4: 19-6722689-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722689G>C , CM000681.2:g.6722689G>C GRCh38
NC_000019.9:g.6722700G>C , CM000681.1:g.6722700G>C GRCh37
NC_000019.8:g.6673700G>C NCBI36
NG_009557.1:g.2963C>G , LRG_27:g.2963C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000600744.1:c.-50+752C>G ENSP00000472044.1:n.-50+752C>G
Search 100 bp 5'
Search 100 bp 3'