Canonical Allele Identifier: CA869060803

Gene: GABBR2

Linked Data

• dbSNP Id: rs7857375
• MyVariant Identifiers: chr9:g.101277609G>C (hg19) ; chr9:g.98515327G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98515327G>C , CM000671.2:g.98515327G>C	GRCh38
NC_000009.11:g.101277609G>C , CM000671.1:g.101277609G>C	GRCh37
NC_000009.10:g.100317430G>C	NCBI36
NG_016426.1:g.198871C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000259455.4:c.631-18813C>G MANE Select	ENSP00000259455.2:n.631-18813C>G
ENST00000637410.1:n.409-18813C>G
ENST00000259455.3:c.631-18813C>G	ENSP00000259455.2:n.631-18813C>G
ENST00000477471.1:n.418-18813C>G
ENST00000634227.1:n.405-18813C>G
ENST00000634919.1:n.306+667C>G
NM_005458.7:c.631-18813C>G	NP_005449.5:n.631-18813C>G
XM_005252316.3:c.-144-18813C>G	XP_005252373.1:n.-144-18813C>G
XM_005252316.5:c.-144-18813C>G	XP_005252373.1:n.-144-18813C>G
XM_017015331.2:c.337-18813C>G	XP_016870820.1:n.337-18813C>G
NM_005458.8:c.631-18813C>G MANE Select	NP_005449.5:n.631-18813C>G