Canonical Allele Identifier: CA466527214
Gene: GABBR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.101340232G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98577950G>T , CM000671.2:g.98577950G>T GRCh38
NC_000009.11:g.101340232G>T , CM000671.1:g.101340232G>T GRCh37
NC_000009.10:g.100380053G>T NCBI36
NG_016426.1:g.136248C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.444C>A MANE Select ENSP00000259455.2:p.Gly148=
ENST00000637410.1:n.222C>A
ENST00000637717.1:c.60C>A ENSP00000490789.1:p.Gly20=
ENST00000259455.3:c.444C>A ENSP00000259455.2:p.Gly148=
ENST00000634227.1:n.218C>A
NM_005458.7:c.444C>A NP_005449.5:p.Gly148=
NM_005458.8:c.444C>A MANE Select NP_005449.5:p.Gly148=
Search 100 bp 5'
Search 100 bp 3'