Canonical Allele Identifier: CA99074772
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs917982177
gnomAD v3: 4-71784847-G-C
gnomAD v4: 4-71784847-G-C
MyVariant Identifiers: chr4:g.72650564G>C (hg19) chr4:g.71784847G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784847G>C , CM000666.2:g.71784847G>C GRCh38
NC_000004.11:g.72650564G>C , CM000666.1:g.72650564G>C GRCh37
NC_000004.10:g.72869428G>C NCBI36
NG_012837.2:g.25674C>G
NG_012837.3:g.25674C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-793C>G ENSP00000421725.1:n.22-793C>G
ENST00000506245.1:c.-36-793C>G ENSP00000426718.1:n.-36-793C>G
NM_001204306.1:c.-36-793C>G NP_001191235.1:n.-36-793C>G
NM_001204307.1:c.22-793C>G NP_001191236.1:n.22-793C>G
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