Canonical Allele Identifier: CA99058419
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs566257319
gnomAD v2: 4-72609455-T-C
gnomAD v3: 4-71743738-T-C
gnomAD v4: 4-71743738-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71743738T>C , CM000666.2:g.71743738T>C GRCh38
NC_000004.11:g.72609455T>C , CM000666.1:g.72609455T>C GRCh37
NC_000004.10:g.72828319T>C NCBI36
NG_012837.2:g.66783A>G
NG_012837.3:g.66783A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.*26-1868A>G MANE Select ENSP00000273951.8:n.*26-1868A>G
ENST00000273951.12:c.*26-1868A>G ENSP00000273951.8:n.*26-1868A>G
ENST00000503364.5:n.124-1868A>G
ENST00000503472.5:n.1335-1868A>G
ENST00000504199.5:c.*26-1868A>G ENSP00000421725.1:n.*26-1868A>G
ENST00000509740.5:c.*274-1868A>G ENSP00000422664.1:n.*274-1868A>G
ENST00000513476.5:c.1396-1868A>G ENSP00000426683.1:n.1396-1868A>G
NM_000583.3:c.*26-1868A>G NP_000574.2:n.*26-1868A>G
NM_001204306.1:c.*26-1868A>G NP_001191235.1:n.*26-1868A>G
NM_001204307.1:c.*26-1868A>G NP_001191236.1:n.*26-1868A>G
XM_006714177.2:c.*40-1868A>G XP_006714240.1:n.*40-1868A>G
XM_006714177.3:c.*40-1868A>G XP_006714240.1:n.*40-1868A>G
NM_000583.4:c.*26-1868A>G MANE Select NP_000574.2:n.*26-1868A>G