Canonical Allele Identifier: CA439795812

Gene: GC

Linked Data

• dbSNP Id: rs1741789746
• MyVariant Identifiers: chr4:g.72622539A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756822A>T , CM000666.2:g.71756822A>T	GRCh38
NC_000004.11:g.72622539A>T , CM000666.1:g.72622539A>T	GRCh37
NC_000004.10:g.72841403A>T	NCBI36
NG_012837.2:g.53699T>A
NG_012837.3:g.53699T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.924T>A MANE Select	ENSP00000273951.8:p.Val308=
ENST00000273951.12:c.924T>A	ENSP00000273951.8:p.Val308=
ENST00000503472.5:n.808T>A
ENST00000504199.5:c.981T>A	ENSP00000421725.1:p.Val327=
ENST00000509740.5:c.924T>A	ENSP00000422664.1:p.Val308=
ENST00000513476.5:c.924T>A	ENSP00000426683.1:p.Val308=
NM_000583.3:c.924T>A	NP_000574.2:p.Val308=
NM_001204306.1:c.924T>A	NP_001191235.1:p.Val308=
NM_001204307.1:c.981T>A	NP_001191236.1:p.Val327=
XM_006714177.2:c.924T>A	XP_006714240.1:p.Val308=
XM_006714177.3:c.924T>A	XP_006714240.1:p.Val308=
NM_000583.4:c.924T>A MANE Select	NP_000574.2:p.Val308=