Canonical Allele Identifier: CA1610190138

Gene: GCM2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10874358G= , CM000668.2:g.10874358G=	GRCh38
NC_000006.11:g.10874591G= , CM000668.1:g.10874591G=	GRCh37
NC_000006.10:g.10982577G=	NCBI36
NG_008970.1:g.12508C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379491.5:c.1158C= MANE Select	ENSP00000368805.4:p.Thr386=
ENST00000379491.4:c.1158C=	ENSP00000368805.4:p.Thr386=
ENST00000480294.1:c.101-17155G=	ENSP00000417929.1:n.101-17155G=
NM_004752.3:c.1158C=	NP_004743.1:p.Thr386=
XM_011514991.1:c.1158C=	XP_011513293.1:p.Thr386=
NM_004752.4:c.1158C= MANE Select	NP_004743.1:p.Thr386=