Canonical Allele Identifier: CA197076883
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs557015103
MyVariant Identifiers: chr9:g.101303848T>C (hg19) chr9:g.98541566T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541566T>C , CM000671.2:g.98541566T>C GRCh38
NC_000009.11:g.101303848T>C , CM000671.1:g.101303848T>C GRCh37
NC_000009.10:g.100343669T>C NCBI36
NG_016426.1:g.172632A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.630+307A>G MANE Select ENSP00000259455.2:n.630+307A>G
ENST00000637410.1:n.408+307A>G
ENST00000259455.3:c.630+307A>G ENSP00000259455.2:n.630+307A>G
ENST00000477471.1:n.417+307A>G
ENST00000634227.1:n.404+307A>G
NM_005458.7:c.630+307A>G NP_005449.5:n.630+307A>G
XM_017015331.2:c.336+307A>G XP_016870820.1:n.336+307A>G
NM_005458.8:c.630+307A>G MANE Select NP_005449.5:n.630+307A>G
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