Canonical Allele Identifier: CA2706157495

Gene: GC

Linked Data

• dbSNP Id: rs202036405

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756090_71756093dup , CM000666.2:g.71756090_71756093dup	GRCh38
NC_000004.11:g.72621807_72621810dup , CM000666.1:g.72621807_72621810dup	GRCh37
NC_000004.10:g.72840671_72840674dup	NCBI36
NG_012837.2:g.54431_54434dup
NG_012837.3:g.54431_54434dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.1034+622_1034+625dup MANE Select	ENSP00000273951.8:n.1034+622_1034+625dup
ENST00000273951.12:c.1034+622_1034+625dup	ENSP00000273951.8:n.1034+622_1034+625dup
ENST00000503472.5:n.918+622_918+625dup
ENST00000504199.5:c.1091+622_1091+625dup	ENSP00000421725.1:n.1091+622_1091+625dup
ENST00000509740.5:c.1034+622_1034+625dup	ENSP00000422664.1:n.1034+622_1034+625dup
ENST00000513476.5:c.1034+622_1034+625dup	ENSP00000426683.1:n.1034+622_1034+625dup
NM_000583.3:c.1034+622_1034+625dup	NP_000574.2:n.1034+622_1034+625dup
NM_001204306.1:c.1034+622_1034+625dup	NP_001191235.1:n.1034+622_1034+625dup
NM_001204307.1:c.1091+622_1091+625dup	NP_001191236.1:n.1091+622_1091+625dup
XM_006714177.2:c.1034+622_1034+625dup	XP_006714240.1:n.1034+622_1034+625dup
XM_006714177.3:c.1034+622_1034+625dup	XP_006714240.1:n.1034+622_1034+625dup
NM_000583.4:c.1034+622_1034+625dup MANE Select	NP_000574.2:n.1034+622_1034+625dup