Canonical Allele Identifier: CA2670941981

Gene: GC

Linked Data

• gnomAD v4: 4-71756956-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756956A>T , CM000666.2:g.71756956A>T	GRCh38
NC_000004.11:g.72622673A>T , CM000666.1:g.72622673A>T	GRCh37
NC_000004.10:g.72841537A>T	NCBI36
NG_012837.2:g.53565T>A
NG_012837.3:g.53565T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.832-42T>A MANE Select	ENSP00000273951.8:n.832-42T>A
ENST00000273951.12:c.832-42T>A	ENSP00000273951.8:n.832-42T>A
ENST00000503472.5:n.716-42T>A
ENST00000504199.5:c.889-42T>A	ENSP00000421725.1:n.889-42T>A
ENST00000509740.5:c.832-42T>A	ENSP00000422664.1:n.832-42T>A
ENST00000513476.5:c.832-42T>A	ENSP00000426683.1:n.832-42T>A
NM_000583.3:c.832-42T>A	NP_000574.2:n.832-42T>A
NM_001204306.1:c.832-42T>A	NP_001191235.1:n.832-42T>A
NM_001204307.1:c.889-42T>A	NP_001191236.1:n.889-42T>A
XM_006714177.2:c.832-42T>A	XP_006714240.1:n.832-42T>A
XM_006714177.3:c.832-42T>A	XP_006714240.1:n.832-42T>A
NM_000583.4:c.832-42T>A MANE Select	NP_000574.2:n.832-42T>A