Canonical Allele Identifier: CA466527068
Gene: GABBR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.101304314A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542032A>C , CM000671.2:g.98542032A>C GRCh38
NC_000009.11:g.101304314A>C , CM000671.1:g.101304314A>C GRCh37
NC_000009.10:g.100344135A>C NCBI36
NG_016426.1:g.172166T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.471T>G MANE Select ENSP00000259455.2:p.Ala157=
ENST00000637410.1:n.249T>G
ENST00000637717.1:c.87T>G ENSP00000490789.1:p.Ala29=
ENST00000638001.1:n.81T>G
ENST00000259455.3:c.471T>G ENSP00000259455.2:p.Ala157=
ENST00000477471.1:n.258T>G
ENST00000634227.1:n.245T>G
NM_005458.7:c.471T>G NP_005449.5:p.Ala157=
XM_017015331.2:c.177T>G XP_016870820.1:p.Ala59=
NM_005458.8:c.471T>G MANE Select NP_005449.5:p.Ala157=