Canonical Allele Identifier: CA1467354811
Gene: GC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71790665T= , CM000666.2:g.71790665T= GRCh38
NC_000004.11:g.72656382T= , CM000666.1:g.72656382T= GRCh37
NC_000004.10:g.72875246T= NCBI36
NG_012837.2:g.19856A=
NG_012837.3:g.19856A=

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-6611A= ENSP00000421725.1:n.22-6611A=
NM_001204306.1:c.-36-6611A= NP_001191235.1:n.-36-6611A=
NM_001204307.1:c.22-6611A= NP_001191236.1:n.22-6611A=
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