Canonical Allele Identifier: CA869067473
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1414519855

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98380458G>C , CM000671.2:g.98380458G>C GRCh38
NC_000009.11:g.101142740G>C , CM000671.1:g.101142740G>C GRCh37
NC_000009.10:g.100182561G>C NCBI36
NG_016426.1:g.333740C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000259455.4:c.1662+5182C>G MANE Select ENSP00000259455.2:n.1662+5182C>G
ENST00000637410.1:n.1440+5182C>G
ENST00000259455.3:c.1662+5182C>G ENSP00000259455.2:n.1662+5182C>G
ENST00000634314.1:n.167+5182C>G
NM_005458.7:c.1662+5182C>G NP_005449.5:n.1662+5182C>G
XM_005252316.3:c.888+5182C>G XP_005252373.1:n.888+5182C>G
XM_005252316.5:c.888+5182C>G XP_005252373.1:n.888+5182C>G
XM_017015331.2:c.1368+5182C>G XP_016870820.1:n.1368+5182C>G
XM_017015332.2:c.888+5182C>G XP_016870821.1:n.888+5182C>G
NM_005458.8:c.1662+5182C>G MANE Select NP_005449.5:n.1662+5182C>G