Canonical Allele Identifier: CA439795775

Gene: GC

Linked Data

• MyVariant Identifiers: chr4:g.72622476G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756759G>T , CM000666.2:g.71756759G>T	GRCh38
NC_000004.11:g.72622476G>T , CM000666.1:g.72622476G>T	GRCh37
NC_000004.10:g.72841340G>T	NCBI36
NG_012837.2:g.53762C>A
NG_012837.3:g.53762C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.987C>A MANE Select	ENSP00000273951.8:p.Pro329=
ENST00000273951.12:c.987C>A	ENSP00000273951.8:p.Pro329=
ENST00000503472.5:n.871C>A
ENST00000504199.5:c.1044C>A	ENSP00000421725.1:p.Pro348=
ENST00000509740.5:c.987C>A	ENSP00000422664.1:p.Pro329=
ENST00000513476.5:c.987C>A	ENSP00000426683.1:p.Pro329=
NM_000583.3:c.987C>A	NP_000574.2:p.Pro329=
NM_001204306.1:c.987C>A	NP_001191235.1:p.Pro329=
NM_001204307.1:c.1044C>A	NP_001191236.1:p.Pro348=
XM_006714177.2:c.987C>A	XP_006714240.1:p.Pro329=
XM_006714177.3:c.987C>A	XP_006714240.1:p.Pro329=
NM_000583.4:c.987C>A MANE Select	NP_000574.2:p.Pro329=