Canonical Allele Identifier: CA11649933
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs2282679

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71742666T>G , CM000666.2:g.71742666T>G GRCh38
NC_000004.11:g.72608383T>G , CM000666.1:g.72608383T>G GRCh37
NC_000004.10:g.72827247T>G NCBI36
NG_012837.2:g.67855A>C
NG_012837.3:g.67855A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.*26-796A>C MANE Select ENSP00000273951.8:p.=
ENST00000273951.12:c.*26-796A>C ENSP00000273951.8:p.=
ENST00000503364.5:n.124-796A>C
ENST00000503472.5:n.1335-796A>C
ENST00000504199.5:c.*26-796A>C ENSP00000421725.1:p.=
ENST00000509740.5:c.*274-796A>C ENSP00000422664.1:p.=
ENST00000513476.5:c.1396-796A>C ENSP00000426683.1:p.=
NM_000583.3:c.*26-796A>C NP_000574.2:p.=
NM_001204306.1:c.*26-796A>C NP_001191235.1:p.=
NM_001204307.1:c.*26-796A>C NP_001191236.1:p.=
XM_006714177.2:c.*40-796A>C XP_006714240.1:p.=
XM_006714177.3:c.*40-796A>C XP_006714240.1:p.=
NM_000583.4:c.*26-796A>C MANE Select NP_000574.2:p.=