Canonical Allele Identifier: CA869072087
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1369360717
MyVariant Identifiers: chr9:g.101304645T>G (hg19) chr9:g.98542363T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542363T>G , CM000671.2:g.98542363T>G GRCh38
NC_000009.11:g.101304645T>G , CM000671.1:g.101304645T>G GRCh37
NC_000009.10:g.100344466T>G NCBI36
NG_016426.1:g.171835A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.460-320A>C MANE Select ENSP00000259455.2:n.460-320A>C
ENST00000637410.1:n.238-320A>C
ENST00000637717.1:c.76-320A>C ENSP00000490789.1:n.76-320A>C
ENST00000638001.1:n.70-320A>C
ENST00000259455.3:c.460-320A>C ENSP00000259455.2:n.460-320A>C
ENST00000477471.1:n.247-320A>C
ENST00000634227.1:n.234-320A>C
NM_005458.7:c.460-320A>C NP_005449.5:n.460-320A>C
XM_017015331.2:c.166-320A>C XP_016870820.1:n.166-320A>C
NM_005458.8:c.460-320A>C MANE Select NP_005449.5:n.460-320A>C
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