Canonical Allele Identifier: CA1866993872
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1828305623
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541599A>G , CM000671.2:g.98541599A>G GRCh38
NC_000009.11:g.101303881A>G , CM000671.1:g.101303881A>G GRCh37
NC_000009.10:g.100343702A>G NCBI36
NG_016426.1:g.172599T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.630+274T>C MANE Select ENSP00000259455.2:n.630+274T>C
ENST00000637410.1:n.408+274T>C
ENST00000259455.3:c.630+274T>C ENSP00000259455.2:n.630+274T>C
ENST00000477471.1:n.417+274T>C
ENST00000634227.1:n.404+274T>C
NM_005458.7:c.630+274T>C NP_005449.5:n.630+274T>C
XM_017015331.2:c.336+274T>C XP_016870820.1:n.336+274T>C
NM_005458.8:c.630+274T>C MANE Select NP_005449.5:n.630+274T>C
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