Canonical Allele Identifier: CA993061123
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1968210207
gnomAD v3: 19-6722735-C-G
gnomAD v4: 19-6722735-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722735C>G , CM000681.2:g.6722735C>G GRCh38
NC_000019.9:g.6722746C>G , CM000681.1:g.6722746C>G GRCh37
NC_000019.8:g.6673746C>G NCBI36
NG_009557.1:g.2917G>C , LRG_27:g.2917G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000600744.1:c.-50+706G>C ENSP00000472044.1:n.-50+706G>C
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