Canonical Allele Identifier: CA1467385673

Gene: GC

Linked Data

• dbSNP Id: rs1742772899

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71784131T>A , CM000666.2:g.71784131T>A	GRCh38
NC_000004.11:g.72649848T>A , CM000666.1:g.72649848T>A	GRCh37
NC_000004.10:g.72868712T>A	NCBI36
NG_012837.2:g.26390A>T
NG_012837.3:g.26390A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.12:c.-113A>T	ENSP00000273951.8:n.-113A>T
ENST00000504199.5:c.22-77A>T	ENSP00000421725.1:n.22-77A>T
ENST00000506245.1:c.-36-77A>T	ENSP00000426718.1:n.-36-77A>T
NM_000583.3:c.-113A>T	NP_000574.2:n.-113A>T
NM_001204306.1:c.-36-77A>T	NP_001191235.1:n.-36-77A>T
NM_001204307.1:c.22-77A>T	NP_001191236.1:n.22-77A>T
XM_006714177.2:c.-113A>T	XP_006714240.1:n.-113A>T