Canonical Allele Identifier: CA1467385979
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs1742795140
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784860G>T , CM000666.2:g.71784860G>T GRCh38
NC_000004.11:g.72650577G>T , CM000666.1:g.72650577G>T GRCh37
NC_000004.10:g.72869441G>T NCBI36
NG_012837.2:g.25661C>A
NG_012837.3:g.25661C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000504199.5:c.22-806C>A ENSP00000421725.1:n.22-806C>A
ENST00000506245.1:c.-36-806C>A ENSP00000426718.1:n.-36-806C>A
NM_001204306.1:c.-36-806C>A NP_001191235.1:n.-36-806C>A
NM_001204307.1:c.22-806C>A NP_001191236.1:n.22-806C>A
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