Canonical Allele Identifier: CA439799386

Gene: GC

Linked Data

• MyVariant Identifiers: chr4:g.72649688A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71783971A>T , CM000666.2:g.71783971A>T	GRCh38
NC_000004.11:g.72649688A>T , CM000666.1:g.72649688A>T	GRCh37
NC_000004.10:g.72868552A>T	NCBI36
NG_012837.2:g.26550T>A
NG_012837.3:g.26550T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.48T>A MANE Select	ENSP00000273951.8:p.Ala16=
ENST00000273951.12:c.48T>A	ENSP00000273951.8:p.Ala16=
ENST00000504199.5:c.105T>A	ENSP00000421725.1:p.Ala35=
ENST00000506245.1:c.48T>A	ENSP00000426718.1:p.Ala16=
ENST00000509740.5:c.48T>A	ENSP00000422664.1:p.Ala16=
ENST00000513476.5:c.48T>A	ENSP00000426683.1:p.Ala16=
NM_000583.3:c.48T>A	NP_000574.2:p.Ala16=
NM_001204306.1:c.48T>A	NP_001191235.1:p.Ala16=
NM_001204307.1:c.105T>A	NP_001191236.1:p.Ala35=
XM_006714177.2:c.48T>A	XP_006714240.1:p.Ala16=
XM_006714177.3:c.48T>A	XP_006714240.1:p.Ala16=
NM_000583.4:c.48T>A MANE Select	NP_000574.2:p.Ala16=