Canonical Allele Identifier: CA1866994598
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1828322795

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542385_98542386insG , CM000671.2:g.98542385_98542386insG GRCh38
NC_000009.11:g.101304667_101304668insG , CM000671.1:g.101304667_101304668insG GRCh37
NC_000009.10:g.100344488_100344489insG NCBI36
NG_016426.1:g.171812_171813insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.460-343_460-342insC MANE Select ENSP00000259455.2:n.460-343_460-342insC
ENST00000637410.1:n.238-343_238-342insC
ENST00000637717.1:c.76-343_76-342insC ENSP00000490789.1:n.76-343_76-342insC
ENST00000638001.1:n.70-343_70-342insC
ENST00000259455.3:c.460-343_460-342insC ENSP00000259455.2:n.460-343_460-342insC
ENST00000477471.1:n.247-343_247-342insC
ENST00000634227.1:n.234-343_234-342insC
NM_005458.7:c.460-343_460-342insC NP_005449.5:n.460-343_460-342insC
XM_017015331.2:c.166-343_166-342insC XP_016870820.1:n.166-343_166-342insC
NM_005458.8:c.460-343_460-342insC MANE Select NP_005449.5:n.460-343_460-342insC