Canonical Allele Identifier: CA466526988
Gene: GABBR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.101304233T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541951T>G , CM000671.2:g.98541951T>G GRCh38
NC_000009.11:g.101304233T>G , CM000671.1:g.101304233T>G GRCh37
NC_000009.10:g.100344054T>G NCBI36
NG_016426.1:g.172247A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.552A>C MANE Select ENSP00000259455.2:p.Pro184=
ENST00000637410.1:n.330A>C
ENST00000637717.1:c.168A>C ENSP00000490789.1:p.Pro56=
ENST00000259455.3:c.552A>C ENSP00000259455.2:p.Pro184=
ENST00000477471.1:n.339A>C
ENST00000634227.1:n.326A>C
NM_005458.7:c.552A>C NP_005449.5:p.Pro184=
XM_017015331.2:c.258A>C XP_016870820.1:p.Pro86=
NM_005458.8:c.552A>C MANE Select NP_005449.5:p.Pro184=
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