Canonical Allele Identifier: CA99074814
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs1030162871
gnomAD v3: 4-71785031-G-A
gnomAD v4: 4-71785031-G-A
MyVariant Identifiers: chr4:g.71785031G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71785031G>A , CM000666.2:g.71785031G>A GRCh38
NC_000004.11:g.72650748G>A , CM000666.1:g.72650748G>A GRCh37
NC_000004.10:g.72869612G>A NCBI36
NG_012837.2:g.25490C>T
NG_012837.3:g.25490C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-977C>T ENSP00000421725.1:n.22-977C>T
ENST00000506245.1:c.-37+889C>T ENSP00000426718.1:n.-37+889C>T
NM_001204306.1:c.-36-977C>T NP_001191235.1:n.-36-977C>T
NM_001204307.1:c.22-977C>T NP_001191236.1:n.22-977C>T