Canonical Allele Identifier: CA798109992
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs1405013875
gnomAD v3: 4-71784836-G-A
gnomAD v4: 4-71784836-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784836G>A , CM000666.2:g.71784836G>A GRCh38
NC_000004.11:g.72650553G>A , CM000666.1:g.72650553G>A GRCh37
NC_000004.10:g.72869417G>A NCBI36
NG_012837.2:g.25685C>T
NG_012837.3:g.25685C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-782C>T ENSP00000421725.1:n.22-782C>T
ENST00000506245.1:c.-36-782C>T ENSP00000426718.1:n.-36-782C>T
NM_001204306.1:c.-36-782C>T NP_001191235.1:n.-36-782C>T
NM_001204307.1:c.22-782C>T NP_001191236.1:n.22-782C>T