Canonical Allele Identifier: CA1127204980
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1827735152
gnomAD v3: 9-98515279-T-G
gnomAD v4: 9-98515279-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98515279T>G , CM000671.2:g.98515279T>G GRCh38
NC_000009.11:g.101277561T>G , CM000671.1:g.101277561T>G GRCh37
NC_000009.10:g.100317382T>G NCBI36
NG_016426.1:g.198919A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.631-18765A>C MANE Select ENSP00000259455.2:n.631-18765A>C
ENST00000637410.1:n.409-18765A>C
ENST00000259455.3:c.631-18765A>C ENSP00000259455.2:n.631-18765A>C
ENST00000477471.1:n.418-18765A>C
ENST00000634227.1:n.405-18765A>C
ENST00000634919.1:n.306+715A>C
NM_005458.7:c.631-18765A>C NP_005449.5:n.631-18765A>C
XM_005252316.3:c.-144-18765A>C XP_005252373.1:n.-144-18765A>C
XM_005252316.5:c.-144-18765A>C XP_005252373.1:n.-144-18765A>C
XM_017015331.2:c.337-18765A>C XP_016870820.1:n.337-18765A>C
NM_005458.8:c.631-18765A>C MANE Select NP_005449.5:n.631-18765A>C