Canonical Allele Identifier: CA869066292

Gene: GABBR2

Linked Data

• dbSNP Id: rs977085933
• gnomAD v3: 9-98443033-A-T
• gnomAD v4: 9-98443033-A-T
• MyVariant Identifiers: chr9:g.101205315A>T (hg19) ; chr9:g.98443033A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98443033A>T , CM000671.2:g.98443033A>T	GRCh38
NC_000009.11:g.101205315A>T , CM000671.1:g.101205315A>T	GRCh37
NC_000009.10:g.100245136A>T	NCBI36
NG_016426.1:g.271165T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259455.4:c.1236+10948T>A MANE Select	ENSP00000259455.2:n.1236+10948T>A
ENST00000637410.1:n.1014+10948T>A
ENST00000259455.3:c.1236+10948T>A	ENSP00000259455.2:n.1236+10948T>A
NM_005458.7:c.1236+10948T>A	NP_005449.5:n.1236+10948T>A
XM_005252316.3:c.462+10948T>A	XP_005252373.1:n.462+10948T>A
XM_005252316.5:c.462+10948T>A	XP_005252373.1:n.462+10948T>A
XM_017015331.2:c.942+10948T>A	XP_016870820.1:n.942+10948T>A
XM_017015332.2:c.462+10948T>A	XP_016870821.1:n.462+10948T>A
NM_005458.8:c.1236+10948T>A MANE Select	NP_005449.5:n.1236+10948T>A