Canonical Allele Identifier: CA1866959847
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1831955949

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98380620G>A , CM000671.2:g.98380620G>A GRCh38
NC_000009.11:g.101142902G>A , CM000671.1:g.101142902G>A GRCh37
NC_000009.10:g.100182723G>A NCBI36
NG_016426.1:g.333578C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000259455.4:c.1662+5020C>T MANE Select ENSP00000259455.2:n.1662+5020C>T
ENST00000637410.1:n.1440+5020C>T
ENST00000259455.3:c.1662+5020C>T ENSP00000259455.2:n.1662+5020C>T
ENST00000634314.1:n.167+5020C>T
NM_005458.7:c.1662+5020C>T NP_005449.5:n.1662+5020C>T
XM_005252316.3:c.888+5020C>T XP_005252373.1:n.888+5020C>T
XM_005252316.5:c.888+5020C>T XP_005252373.1:n.888+5020C>T
XM_017015331.2:c.1368+5020C>T XP_016870820.1:n.1368+5020C>T
XM_017015332.2:c.888+5020C>T XP_016870821.1:n.888+5020C>T
NM_005458.8:c.1662+5020C>T MANE Select NP_005449.5:n.1662+5020C>T