Canonical Allele Identifier: CA1127195493
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1831951962
gnomAD v3: 9-98380447-A-C
gnomAD v4: 9-98380447-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98380447A>C , CM000671.2:g.98380447A>C GRCh38
NC_000009.11:g.101142729A>C , CM000671.1:g.101142729A>C GRCh37
NC_000009.10:g.100182550A>C NCBI36
NG_016426.1:g.333751T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000259455.4:c.1662+5193T>G MANE Select ENSP00000259455.2:n.1662+5193T>G
ENST00000637410.1:n.1440+5193T>G
ENST00000259455.3:c.1662+5193T>G ENSP00000259455.2:n.1662+5193T>G
ENST00000634314.1:n.167+5193T>G
NM_005458.7:c.1662+5193T>G NP_005449.5:n.1662+5193T>G
XM_005252316.3:c.888+5193T>G XP_005252373.1:n.888+5193T>G
XM_005252316.5:c.888+5193T>G XP_005252373.1:n.888+5193T>G
XM_017015331.2:c.1368+5193T>G XP_016870820.1:n.1368+5193T>G
XM_017015332.2:c.888+5193T>G XP_016870821.1:n.888+5193T>G
NM_005458.8:c.1662+5193T>G MANE Select NP_005449.5:n.1662+5193T>G