Canonical Allele Identifier: CA993061085
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1968209004
gnomAD v3: 19-6722635-G-A
gnomAD v4: 19-6722635-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722635G>A , CM000681.2:g.6722635G>A GRCh38
NC_000019.9:g.6722646G>A , CM000681.1:g.6722646G>A GRCh37
NC_000019.8:g.6673646G>A NCBI36
NG_009557.1:g.3017C>T , LRG_27:g.3017C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000600744.1:c.-50+806C>T ENSP00000472044.1:n.-50+806C>T
Search 100 bp 5'
Search 100 bp 3'