Canonical Allele Identifier: CA1866885589

Gene: GABBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98341417C= , CM000671.2:g.98341417C=	GRCh38
NC_000009.11:g.101103699C= , CM000671.1:g.101103699C=	GRCh37
NC_000009.10:g.100143520C=	NCBI36
NG_016426.1:g.372781G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000259455.4:c.1893+21298G= MANE Select	ENSP00000259455.2:n.1893+21298G=
ENST00000637410.1:n.1671+21298G=
ENST00000259455.3:c.1893+21298G=	ENSP00000259455.2:n.1893+21298G=
ENST00000634457.1:c.231+21298G=	ENSP00000489352.1:n.231+21298G=
ENST00000635462.1:n.388+21298G=
NM_005458.7:c.1893+21298G=	NP_005449.5:n.1893+21298G=
XM_005252316.3:c.1119+21298G=	XP_005252373.1:n.1119+21298G=
XM_005252316.5:c.1119+21298G=	XP_005252373.1:n.1119+21298G=
XM_017015331.2:c.1599+21298G=	XP_016870820.1:n.1599+21298G=
XM_017015332.2:c.1119+21298G=	XP_016870821.1:n.1119+21298G=
NM_005458.8:c.1893+21298G= MANE Select	NP_005449.5:n.1893+21298G=