Canonical Allele Identifier: CA1866994622
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1828323262

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542401A>C , CM000671.2:g.98542401A>C GRCh38
NC_000009.11:g.101304683A>C , CM000671.1:g.101304683A>C GRCh37
NC_000009.10:g.100344504A>C NCBI36
NG_016426.1:g.171797T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.460-358T>G MANE Select ENSP00000259455.2:n.460-358T>G
ENST00000637410.1:n.238-358T>G
ENST00000637717.1:c.76-358T>G ENSP00000490789.1:n.76-358T>G
ENST00000638001.1:n.70-358T>G
ENST00000259455.3:c.460-358T>G ENSP00000259455.2:n.460-358T>G
ENST00000477471.1:n.247-358T>G
ENST00000634227.1:n.234-358T>G
NM_005458.7:c.460-358T>G NP_005449.5:n.460-358T>G
XM_017015331.2:c.166-358T>G XP_016870820.1:n.166-358T>G
NM_005458.8:c.460-358T>G MANE Select NP_005449.5:n.460-358T>G