Canonical Allele Identifier: CA1127205004
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1827735911
gnomAD v3: 9-98515307-A-G
gnomAD v4: 9-98515307-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98515307A>G , CM000671.2:g.98515307A>G GRCh38
NC_000009.11:g.101277589A>G , CM000671.1:g.101277589A>G GRCh37
NC_000009.10:g.100317410A>G NCBI36
NG_016426.1:g.198891T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000259455.4:c.631-18793T>C MANE Select ENSP00000259455.2:n.631-18793T>C
ENST00000637410.1:n.409-18793T>C
ENST00000259455.3:c.631-18793T>C ENSP00000259455.2:n.631-18793T>C
ENST00000477471.1:n.418-18793T>C
ENST00000634227.1:n.405-18793T>C
ENST00000634919.1:n.306+687T>C
NM_005458.7:c.631-18793T>C NP_005449.5:n.631-18793T>C
XM_005252316.3:c.-144-18793T>C XP_005252373.1:n.-144-18793T>C
XM_005252316.5:c.-144-18793T>C XP_005252373.1:n.-144-18793T>C
XM_017015331.2:c.337-18793T>C XP_016870820.1:n.337-18793T>C
NM_005458.8:c.631-18793T>C MANE Select NP_005449.5:n.631-18793T>C