Canonical Allele Identifier: CA1127183467
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1826056989
gnomAD v3: 9-98442926-A-C
gnomAD v4: 9-98442926-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98442926A>C , CM000671.2:g.98442926A>C GRCh38
NC_000009.11:g.101205208A>C , CM000671.1:g.101205208A>C GRCh37
NC_000009.10:g.100245029A>C NCBI36
NG_016426.1:g.271272T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.1236+11055T>G MANE Select ENSP00000259455.2:n.1236+11055T>G
ENST00000637410.1:n.1014+11055T>G
ENST00000259455.3:c.1236+11055T>G ENSP00000259455.2:n.1236+11055T>G
NM_005458.7:c.1236+11055T>G NP_005449.5:n.1236+11055T>G
XM_005252316.3:c.462+11055T>G XP_005252373.1:n.462+11055T>G
XM_005252316.5:c.462+11055T>G XP_005252373.1:n.462+11055T>G
XM_017015331.2:c.942+11055T>G XP_016870820.1:n.942+11055T>G
XM_017015332.2:c.462+11055T>G XP_016870821.1:n.462+11055T>G
NM_005458.8:c.1236+11055T>G MANE Select NP_005449.5:n.1236+11055T>G