Canonical Allele Identifier: CA99074746
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs138108427
gnomAD v2: 4-72650393-G-A
gnomAD v3: 4-71784676-G-A
gnomAD v4: 4-71784676-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784676G>A , CM000666.2:g.71784676G>A GRCh38
NC_000004.11:g.72650393G>A , CM000666.1:g.72650393G>A GRCh37
NC_000004.10:g.72869257G>A NCBI36
NG_012837.2:g.25845C>T
NG_012837.3:g.25845C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000504199.5:c.22-622C>T ENSP00000421725.1:n.22-622C>T
ENST00000506245.1:c.-36-622C>T ENSP00000426718.1:n.-36-622C>T
NM_001204306.1:c.-36-622C>T NP_001191235.1:n.-36-622C>T
NM_001204307.1:c.22-622C>T NP_001191236.1:n.22-622C>T