Canonical Allele Identifier: CA1866993851
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs184349896
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541565G>T , CM000671.2:g.98541565G>T GRCh38
NC_000009.11:g.101303847G>T , CM000671.1:g.101303847G>T GRCh37
NC_000009.10:g.100343668G>T NCBI36
NG_016426.1:g.172633C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.630+308C>A MANE Select ENSP00000259455.2:n.630+308C>A
ENST00000637410.1:n.408+308C>A
ENST00000259455.3:c.630+308C>A ENSP00000259455.2:n.630+308C>A
ENST00000477471.1:n.417+308C>A
ENST00000634227.1:n.404+308C>A
NM_005458.7:c.630+308C>A NP_005449.5:n.630+308C>A
XM_017015331.2:c.336+308C>A XP_016870820.1:n.336+308C>A
NM_005458.8:c.630+308C>A MANE Select NP_005449.5:n.630+308C>A
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