Canonical Allele Identifier: CA869066280

Gene: GABBR2

Linked Data

• dbSNP Id: rs1317605576
• MyVariant Identifiers: chr9:g.101205253_101205256del (hg19) ; chr9:g.98442971_98442974del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98442972_98442975del , CM000671.2:g.98442972_98442975del	GRCh38
NC_000009.11:g.101205254_101205257del , CM000671.1:g.101205254_101205257del	GRCh37
NC_000009.10:g.100245075_100245078del	NCBI36
NG_016426.1:g.271224_271227del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259455.4:c.1236+11007_1236+11010del MANE Select	ENSP00000259455.2:n.1236+11007_1236+11010del
ENST00000637410.1:n.1014+11007_1014+11010del
ENST00000259455.3:c.1236+11007_1236+11010del	ENSP00000259455.2:n.1236+11007_1236+11010del
NM_005458.7:c.1236+11007_1236+11010del	NP_005449.5:n.1236+11007_1236+11010del
XM_005252316.3:c.462+11007_462+11010del	XP_005252373.1:n.462+11007_462+11010del
XM_005252316.5:c.462+11007_462+11010del	XP_005252373.1:n.462+11007_462+11010del
XM_017015331.2:c.942+11007_942+11010del	XP_016870820.1:n.942+11007_942+11010del
XM_017015332.2:c.462+11007_462+11010del	XP_016870821.1:n.462+11007_462+11010del
NM_005458.8:c.1236+11007_1236+11010del MANE Select	NP_005449.5:n.1236+11007_1236+11010del