Canonical Allele Identifier: CA2670943551
Gene: GC HGNC NCBI

Linked Data

gnomAD v4: 4-71783956-CT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71783958del , CM000666.2:g.71783958del GRCh38
NC_000004.11:g.72649675del , CM000666.1:g.72649675del GRCh37
NC_000004.10:g.72868539del NCBI36
NG_012837.2:g.26564del
NG_012837.3:g.26564del

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.58+4del MANE Select ENSP00000273951.8:n.58+4del
ENST00000273951.12:c.58+4del ENSP00000273951.8:n.58+4del
ENST00000504199.5:c.115+4del ENSP00000421725.1:n.115+4del
ENST00000506245.1:c.58+4del ENSP00000426718.1:n.58+4del
ENST00000509740.5:c.58+4del ENSP00000422664.1:n.58+4del
ENST00000513476.5:c.58+4del ENSP00000426683.1:n.58+4del
NM_000583.3:c.58+4del NP_000574.2:n.58+4del
NM_001204306.1:c.58+4del NP_001191235.1:n.58+4del
NM_001204307.1:c.115+4del NP_001191236.1:n.115+4del
XM_006714177.2:c.58+4del XP_006714240.1:n.58+4del
XM_006714177.3:c.58+4del XP_006714240.1:n.58+4del
NM_000583.4:c.58+4del MANE Select NP_000574.2:n.58+4del
Search 100 bp 5'
Search 100 bp 3'