Canonical Allele Identifier: CA304807435
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs529411095
gnomAD v2: 19-6722621-A-G
gnomAD v3: 19-6722610-A-G
gnomAD v4: 19-6722610-A-G
MyVariant Identifiers: chr19:g.6722621A>G (hg19) chr19:g.6722610A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722610A>G , CM000681.2:g.6722610A>G GRCh38
NC_000019.9:g.6722621A>G , CM000681.1:g.6722621A>G GRCh37
NC_000019.8:g.6673621A>G NCBI36
NG_009557.1:g.3042T>C , LRG_27:g.3042T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000600744.1:c.-50+831T>C ENSP00000472044.1:n.-50+831T>C
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