Canonical Allele Identifier: CA1866994313
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1828314650
gnomAD v4: 9-98542094-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542094T>C , CM000671.2:g.98542094T>C GRCh38
NC_000009.11:g.101304376T>C , CM000671.1:g.101304376T>C GRCh37
NC_000009.10:g.100344197T>C NCBI36
NG_016426.1:g.172104A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.460-51A>G MANE Select ENSP00000259455.2:n.460-51A>G
ENST00000637410.1:n.238-51A>G
ENST00000637717.1:c.76-51A>G ENSP00000490789.1:n.76-51A>G
ENST00000638001.1:n.70-51A>G
ENST00000259455.3:c.460-51A>G ENSP00000259455.2:n.460-51A>G
ENST00000477471.1:n.247-51A>G
ENST00000634227.1:n.234-51A>G
NM_005458.7:c.460-51A>G NP_005449.5:n.460-51A>G
XM_017015331.2:c.166-51A>G XP_016870820.1:n.166-51A>G
NM_005458.8:c.460-51A>G MANE Select NP_005449.5:n.460-51A>G