Canonical Allele Identifier: CA99074807
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs1006578382

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784962_71784965del , CM000666.2:g.71784962_71784965del GRCh38
NC_000004.11:g.72650679_72650682del , CM000666.1:g.72650679_72650682del GRCh37
NC_000004.10:g.72869543_72869546del NCBI36
NG_012837.2:g.25561_25564del
NG_012837.3:g.25561_25564del

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-906_22-903del ENSP00000421725.1:n.22-906_22-903del
ENST00000506245.1:c.-36-906_-36-903del ENSP00000426718.1:n.-36-906_-36-903del
NM_001204306.1:c.-36-906_-36-903del NP_001191235.1:n.-36-906_-36-903del
NM_001204307.1:c.22-906_22-903del NP_001191236.1:n.22-906_22-903del