Canonical Allele Identifier: CA1467386070
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs1560710810

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71785075T>C , CM000666.2:g.71785075T>C GRCh38
NC_000004.11:g.72650792T>C , CM000666.1:g.72650792T>C GRCh37
NC_000004.10:g.72869656T>C NCBI36
NG_012837.2:g.25446A>G
NG_012837.3:g.25446A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-1021A>G ENSP00000421725.1:n.22-1021A>G
ENST00000506245.1:c.-37+845A>G ENSP00000426718.1:n.-37+845A>G
NM_001204306.1:c.-36-1021A>G NP_001191235.1:n.-36-1021A>G
NM_001204307.1:c.22-1021A>G NP_001191236.1:n.22-1021A>G