Canonical Allele Identifier: CA798110069
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs1336400510

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784990_71784996del , CM000666.2:g.71784990_71784996del GRCh38
NC_000004.11:g.72650707_72650713del , CM000666.1:g.72650707_72650713del GRCh37
NC_000004.10:g.72869571_72869577del NCBI36
NG_012837.2:g.25527_25533del
NG_012837.3:g.25527_25533del

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-940_22-934del ENSP00000421725.1:n.22-940_22-934del
ENST00000506245.1:c.-37+926_-37+932del ENSP00000426718.1:n.-37+926_-37+932del
NM_001204306.1:c.-36-940_-36-934del NP_001191235.1:n.-36-940_-36-934del
NM_001204307.1:c.22-940_22-934del NP_001191236.1:n.22-940_22-934del