Canonical Allele Identifier: CA99074818
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs11934186
gnomAD v3: 4-71785047-C-T
gnomAD v4: 4-71785047-C-T
MyVariant Identifiers: chr4:g.72650764C>T (hg19) chr4:g.71785047C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71785047C>T , CM000666.2:g.71785047C>T GRCh38
NC_000004.11:g.72650764C>T , CM000666.1:g.72650764C>T GRCh37
NC_000004.10:g.72869628C>T NCBI36
NG_012837.2:g.25474G>A
NG_012837.3:g.25474G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-993G>A ENSP00000421725.1:n.22-993G>A
ENST00000506245.1:c.-37+873G>A ENSP00000426718.1:n.-37+873G>A
NM_001204306.1:c.-36-993G>A NP_001191235.1:n.-36-993G>A
NM_001204307.1:c.22-993G>A NP_001191236.1:n.22-993G>A
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