Canonical Allele Identifier: CA1063992447

Gene: GC

Linked Data

• dbSNP Id: rs1194314285
• gnomAD v3: 4-71755926-C-T
• gnomAD v4: 4-71755926-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71755926C>T , CM000666.2:g.71755926C>T	GRCh38
NC_000004.11:g.72621643C>T , CM000666.1:g.72621643C>T	GRCh37
NC_000004.10:g.72840507C>T	NCBI36
NG_012837.2:g.54595G>A
NG_012837.3:g.54595G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.1034+786G>A MANE Select	ENSP00000273951.8:n.1034+786G>A
ENST00000273951.12:c.1034+786G>A	ENSP00000273951.8:n.1034+786G>A
ENST00000503472.5:n.918+786G>A
ENST00000504199.5:c.1091+786G>A	ENSP00000421725.1:n.1091+786G>A
ENST00000509740.5:c.1034+786G>A	ENSP00000422664.1:n.1034+786G>A
ENST00000513476.5:c.1034+786G>A	ENSP00000426683.1:n.1034+786G>A
NM_000583.3:c.1034+786G>A	NP_000574.2:n.1034+786G>A
NM_001204306.1:c.1034+786G>A	NP_001191235.1:n.1034+786G>A
NM_001204307.1:c.1091+786G>A	NP_001191236.1:n.1091+786G>A
XM_006714177.2:c.1034+786G>A	XP_006714240.1:n.1034+786G>A
XM_006714177.3:c.1034+786G>A	XP_006714240.1:n.1034+786G>A
NM_000583.4:c.1034+786G>A MANE Select	NP_000574.2:n.1034+786G>A