Canonical Allele Identifier: CA1866959670
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98380449T= , CM000671.2:g.98380449T= GRCh38
NC_000009.11:g.101142731T= , CM000671.1:g.101142731T= GRCh37
NC_000009.10:g.100182552T= NCBI36
NG_016426.1:g.333749A=

Transcript Alleles

HGVS Amino-acid change
ENST00000259455.4:c.1662+5191A= MANE Select ENSP00000259455.2:n.1662+5191A=
ENST00000637410.1:n.1440+5191A=
ENST00000259455.3:c.1662+5191A= ENSP00000259455.2:n.1662+5191A=
ENST00000634314.1:n.167+5191A=
NM_005458.7:c.1662+5191A= NP_005449.5:n.1662+5191A=
XM_005252316.3:c.888+5191A= XP_005252373.1:n.888+5191A=
XM_005252316.5:c.888+5191A= XP_005252373.1:n.888+5191A=
XM_017015331.2:c.1368+5191A= XP_016870820.1:n.1368+5191A=
XM_017015332.2:c.888+5191A= XP_016870821.1:n.888+5191A=
NM_005458.8:c.1662+5191A= MANE Select NP_005449.5:n.1662+5191A=