Canonical Allele Identifier: CA1867008269
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1393926683

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98515431T>C , CM000671.2:g.98515431T>C GRCh38
NC_000009.11:g.101277713T>C , CM000671.1:g.101277713T>C GRCh37
NC_000009.10:g.100317534T>C NCBI36
NG_016426.1:g.198767A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000259455.4:c.631-18917A>G MANE Select ENSP00000259455.2:n.631-18917A>G
ENST00000637410.1:n.409-18917A>G
ENST00000259455.3:c.631-18917A>G ENSP00000259455.2:n.631-18917A>G
ENST00000477471.1:n.418-18917A>G
ENST00000634227.1:n.405-18917A>G
ENST00000634919.1:n.306+563A>G
NM_005458.7:c.631-18917A>G NP_005449.5:n.631-18917A>G
XM_005252316.3:c.-144-18917A>G XP_005252373.1:n.-144-18917A>G
XM_005252316.5:c.-144-18917A>G XP_005252373.1:n.-144-18917A>G
XM_017015331.2:c.337-18917A>G XP_016870820.1:n.337-18917A>G
NM_005458.8:c.631-18917A>G MANE Select NP_005449.5:n.631-18917A>G