Canonical Allele Identifier: CA798109910
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs1360950358
gnomAD v3: 4-71784678-C-A
gnomAD v4: 4-71784678-C-A
MyVariant Identifiers: chr4:g.72650395C>A (hg19) chr4:g.71784678C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784678C>A , CM000666.2:g.71784678C>A GRCh38
NC_000004.11:g.72650395C>A , CM000666.1:g.72650395C>A GRCh37
NC_000004.10:g.72869259C>A NCBI36
NG_012837.2:g.25843G>T
NG_012837.3:g.25843G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000504199.5:c.22-624G>T ENSP00000421725.1:n.22-624G>T
ENST00000506245.1:c.-36-624G>T ENSP00000426718.1:n.-36-624G>T
NM_001204306.1:c.-36-624G>T NP_001191235.1:n.-36-624G>T
NM_001204307.1:c.22-624G>T NP_001191236.1:n.22-624G>T
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