Canonical Allele Identifier: CA2544617390
Gene: GC HGNC NCBI

Linked Data

gnomAD v4: 4-71784082-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784082C>A , CM000666.2:g.71784082C>A GRCh38
NC_000004.11:g.72649799C>A , CM000666.1:g.72649799C>A GRCh37
NC_000004.10:g.72868663C>A NCBI36
NG_012837.2:g.26439G>T
NG_012837.3:g.26439G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000273951.12:c.-64G>T ENSP00000273951.8:n.-64G>T
ENST00000504199.5:c.22-28G>T ENSP00000421725.1:n.22-28G>T
ENST00000506245.1:c.-36-28G>T ENSP00000426718.1:n.-36-28G>T
NM_000583.3:c.-64G>T NP_000574.2:n.-64G>T
NM_001204306.1:c.-36-28G>T NP_001191235.1:n.-36-28G>T
NM_001204307.1:c.22-28G>T NP_001191236.1:n.22-28G>T
XM_006714177.2:c.-64G>T XP_006714240.1:n.-64G>T