Canonical Allele Identifier: CA466526943
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1270598084
MyVariant Identifiers: chr9:g.101304161G>A (hg19) chr9:g.98541879G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541879G>A , CM000671.2:g.98541879G>A GRCh38
NC_000009.11:g.101304161G>A , CM000671.1:g.101304161G>A GRCh37
NC_000009.10:g.100343982G>A NCBI36
NG_016426.1:g.172319C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.624C>T MANE Select ENSP00000259455.2:p.Phe208=
ENST00000637410.1:n.402C>T
ENST00000259455.3:c.624C>T ENSP00000259455.2:p.Phe208=
ENST00000477471.1:n.411C>T
ENST00000634227.1:n.398C>T
NM_005458.7:c.624C>T NP_005449.5:p.Phe208=
XM_017015331.2:c.330C>T XP_016870820.1:p.Phe110=
NM_005458.8:c.624C>T MANE Select NP_005449.5:p.Phe208=
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