Canonical Allele Identifier: CA1866885581
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98341401T= , CM000671.2:g.98341401T= GRCh38
NC_000009.11:g.101103683T= , CM000671.1:g.101103683T= GRCh37
NC_000009.10:g.100143504T= NCBI36
NG_016426.1:g.372797A=

Transcript Alleles

HGVS Amino-acid change
ENST00000259455.4:c.1893+21314A= MANE Select ENSP00000259455.2:n.1893+21314A=
ENST00000637410.1:n.1671+21314A=
ENST00000259455.3:c.1893+21314A= ENSP00000259455.2:n.1893+21314A=
ENST00000634457.1:c.231+21314A= ENSP00000489352.1:n.231+21314A=
ENST00000635462.1:n.388+21314A=
NM_005458.7:c.1893+21314A= NP_005449.5:n.1893+21314A=
XM_005252316.3:c.1119+21314A= XP_005252373.1:n.1119+21314A=
XM_005252316.5:c.1119+21314A= XP_005252373.1:n.1119+21314A=
XM_017015331.2:c.1599+21314A= XP_016870820.1:n.1599+21314A=
XM_017015332.2:c.1119+21314A= XP_016870821.1:n.1119+21314A=
NM_005458.8:c.1893+21314A= MANE Select NP_005449.5:n.1893+21314A=