Canonical Allele Identifier: CA197076920

Gene: GABBR2

Linked Data

• dbSNP Id: rs1010451479
• gnomAD v3: 9-98542187-T-C
• gnomAD v4: 9-98542187-T-C
• MyVariant Identifiers: chr9:g.101304469T>C (hg19) ; chr9:g.98542187T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98542187T>C , CM000671.2:g.98542187T>C	GRCh38
NC_000009.11:g.101304469T>C , CM000671.1:g.101304469T>C	GRCh37
NC_000009.10:g.100344290T>C	NCBI36
NG_016426.1:g.172011A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259455.4:c.460-144A>G MANE Select	ENSP00000259455.2:n.460-144A>G
ENST00000637410.1:n.238-144A>G
ENST00000637717.1:c.76-144A>G	ENSP00000490789.1:n.76-144A>G
ENST00000638001.1:n.70-144A>G
ENST00000259455.3:c.460-144A>G	ENSP00000259455.2:n.460-144A>G
ENST00000477471.1:n.247-144A>G
ENST00000634227.1:n.234-144A>G
NM_005458.7:c.460-144A>G	NP_005449.5:n.460-144A>G
XM_017015331.2:c.166-144A>G	XP_016870820.1:n.166-144A>G
NM_005458.8:c.460-144A>G MANE Select	NP_005449.5:n.460-144A>G