Canonical Allele Identifier: CA798110000
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs1321814876
MyVariant Identifiers: chr4:g.72650567A>G (hg19) chr4:g.71784850A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784850A>G , CM000666.2:g.71784850A>G GRCh38
NC_000004.11:g.72650567A>G , CM000666.1:g.72650567A>G GRCh37
NC_000004.10:g.72869431A>G NCBI36
NG_012837.2:g.25671T>C
NG_012837.3:g.25671T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-796T>C ENSP00000421725.1:n.22-796T>C
ENST00000506245.1:c.-36-796T>C ENSP00000426718.1:n.-36-796T>C
NM_001204306.1:c.-36-796T>C NP_001191235.1:n.-36-796T>C
NM_001204307.1:c.22-796T>C NP_001191236.1:n.22-796T>C
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