Canonical Allele Identifier: CA2813447052
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722503G>A , CM000681.2:g.6722503G>A GRCh38
NC_000019.9:g.6722514G>A , CM000681.1:g.6722514G>A GRCh37
NC_000019.8:g.6673514G>A NCBI36
NG_009557.1:g.3149C>T , LRG_27:g.3149C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000600744.1:c.-50+938C>T ENSP00000472044.1:n.-50+938C>T
Search 100 bp 5'
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