Canonical Allele Identifier: CA1127195533
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1831954495
gnomAD v3: 9-98380543-C-T
gnomAD v4: 9-98380543-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98380543C>T , CM000671.2:g.98380543C>T GRCh38
NC_000009.11:g.101142825C>T , CM000671.1:g.101142825C>T GRCh37
NC_000009.10:g.100182646C>T NCBI36
NG_016426.1:g.333655G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000259455.4:c.1662+5097G>A MANE Select ENSP00000259455.2:n.1662+5097G>A
ENST00000637410.1:n.1440+5097G>A
ENST00000259455.3:c.1662+5097G>A ENSP00000259455.2:n.1662+5097G>A
ENST00000634314.1:n.167+5097G>A
NM_005458.7:c.1662+5097G>A NP_005449.5:n.1662+5097G>A
XM_005252316.3:c.888+5097G>A XP_005252373.1:n.888+5097G>A
XM_005252316.5:c.888+5097G>A XP_005252373.1:n.888+5097G>A
XM_017015331.2:c.1368+5097G>A XP_016870820.1:n.1368+5097G>A
XM_017015332.2:c.888+5097G>A XP_016870821.1:n.888+5097G>A
NM_005458.8:c.1662+5097G>A MANE Select NP_005449.5:n.1662+5097G>A