Canonical Allele Identifier: CA1467354801
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs1476605771
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71790635G>C , CM000666.2:g.71790635G>C GRCh38
NC_000004.11:g.72656352G>C , CM000666.1:g.72656352G>C GRCh37
NC_000004.10:g.72875216G>C NCBI36
NG_012837.2:g.19886C>G
NG_012837.3:g.19886C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-6581C>G ENSP00000421725.1:n.22-6581C>G
NM_001204306.1:c.-36-6581C>G NP_001191235.1:n.-36-6581C>G
NM_001204307.1:c.22-6581C>G NP_001191236.1:n.22-6581C>G
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