Canonical Allele Identifier: CA466527207
Gene: GABBR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.101340220C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98577938C>G , CM000671.2:g.98577938C>G GRCh38
NC_000009.11:g.101340220C>G , CM000671.1:g.101340220C>G GRCh37
NC_000009.10:g.100380041C>G NCBI36
NG_016426.1:g.136260G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.456G>C MANE Select ENSP00000259455.2:p.Val152=
ENST00000637410.1:n.234G>C
ENST00000637717.1:c.72G>C ENSP00000490789.1:p.Val24=
ENST00000259455.3:c.456G>C ENSP00000259455.2:p.Val152=
ENST00000634227.1:n.230G>C
NM_005458.7:c.456G>C NP_005449.5:p.Val152=
NM_005458.8:c.456G>C MANE Select NP_005449.5:p.Val152=