Canonical Allele Identifier: CA1467354806
Gene: GC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71790649A= , CM000666.2:g.71790649A= GRCh38
NC_000004.11:g.72656366A= , CM000666.1:g.72656366A= GRCh37
NC_000004.10:g.72875230A= NCBI36
NG_012837.2:g.19872T=
NG_012837.3:g.19872T=

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-6595T= ENSP00000421725.1:n.22-6595T=
NM_001204306.1:c.-36-6595T= NP_001191235.1:n.-36-6595T=
NM_001204307.1:c.22-6595T= NP_001191236.1:n.22-6595T=
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