Canonical Allele Identifier: CA1127195546
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1831955309
gnomAD v3: 9-98380590-T-C
gnomAD v4: 9-98380590-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98380590T>C , CM000671.2:g.98380590T>C GRCh38
NC_000009.11:g.101142872T>C , CM000671.1:g.101142872T>C GRCh37
NC_000009.10:g.100182693T>C NCBI36
NG_016426.1:g.333608A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000259455.4:c.1662+5050A>G MANE Select ENSP00000259455.2:n.1662+5050A>G
ENST00000637410.1:n.1440+5050A>G
ENST00000259455.3:c.1662+5050A>G ENSP00000259455.2:n.1662+5050A>G
ENST00000634314.1:n.167+5050A>G
NM_005458.7:c.1662+5050A>G NP_005449.5:n.1662+5050A>G
XM_005252316.3:c.888+5050A>G XP_005252373.1:n.888+5050A>G
XM_005252316.5:c.888+5050A>G XP_005252373.1:n.888+5050A>G
XM_017015331.2:c.1368+5050A>G XP_016870820.1:n.1368+5050A>G
XM_017015332.2:c.888+5050A>G XP_016870821.1:n.888+5050A>G
NM_005458.8:c.1662+5050A>G MANE Select NP_005449.5:n.1662+5050A>G