Canonical Allele Identifier: CA869071991
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1397141656
gnomAD v3: 9-98542137-A-G
gnomAD v4: 9-98542137-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542137A>G , CM000671.2:g.98542137A>G GRCh38
NC_000009.11:g.101304419A>G , CM000671.1:g.101304419A>G GRCh37
NC_000009.10:g.100344240A>G NCBI36
NG_016426.1:g.172061T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.460-94T>C MANE Select ENSP00000259455.2:n.460-94T>C
ENST00000637410.1:n.238-94T>C
ENST00000637717.1:c.76-94T>C ENSP00000490789.1:n.76-94T>C
ENST00000638001.1:n.70-94T>C
ENST00000259455.3:c.460-94T>C ENSP00000259455.2:n.460-94T>C
ENST00000477471.1:n.247-94T>C
ENST00000634227.1:n.234-94T>C
NM_005458.7:c.460-94T>C NP_005449.5:n.460-94T>C
XM_017015331.2:c.166-94T>C XP_016870820.1:n.166-94T>C
NM_005458.8:c.460-94T>C MANE Select NP_005449.5:n.460-94T>C