Canonical Allele Identifier: CA1866885562

Gene: GABBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98341379T= , CM000671.2:g.98341379T=	GRCh38
NC_000009.11:g.101103661T= , CM000671.1:g.101103661T=	GRCh37
NC_000009.10:g.100143482T=	NCBI36
NG_016426.1:g.372819A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000259455.4:c.1893+21336A= MANE Select	ENSP00000259455.2:n.1893+21336A=
ENST00000637410.1:n.1671+21336A=
ENST00000259455.3:c.1893+21336A=	ENSP00000259455.2:n.1893+21336A=
ENST00000634457.1:c.231+21336A=	ENSP00000489352.1:n.231+21336A=
ENST00000635462.1:n.388+21336A=
NM_005458.7:c.1893+21336A=	NP_005449.5:n.1893+21336A=
XM_005252316.3:c.1119+21336A=	XP_005252373.1:n.1119+21336A=
XM_005252316.5:c.1119+21336A=	XP_005252373.1:n.1119+21336A=
XM_017015331.2:c.1599+21336A=	XP_016870820.1:n.1599+21336A=
XM_017015332.2:c.1119+21336A=	XP_016870821.1:n.1119+21336A=
NM_005458.8:c.1893+21336A= MANE Select	NP_005449.5:n.1893+21336A=