Canonical Allele Identifier: CA884137267
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs756359922
gnomAD v3: 19-6722466-G-T
gnomAD v4: 19-6722466-G-T
MyVariant Identifiers: chr19:g.6722477G>T (hg19) chr19:g.6722466G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722466G>T , CM000681.2:g.6722466G>T GRCh38
NC_000019.9:g.6722477G>T , CM000681.1:g.6722477G>T GRCh37
NC_000019.8:g.6673477G>T NCBI36
NG_009557.1:g.3186C>A , LRG_27:g.3186C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000600744.1:c.-50+975C>A ENSP00000472044.1:n.-50+975C>A
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