Canonical Allele Identifier: CA374351175
Gene: GABBR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.101304309G>C (hg19) chr9:g.98542027G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542027G>C , CM000671.2:g.98542027G>C GRCh38
NC_000009.11:g.101304309G>C , CM000671.1:g.101304309G>C GRCh37
NC_000009.10:g.100344130G>C NCBI36
NG_016426.1:g.172171C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.476C>G MANE Select ENSP00000259455.2:p.Thr159Ser
ENST00000637410.1:n.254C>G
ENST00000637717.1:c.92C>G ENSP00000490789.1:p.Thr31Ser
ENST00000638001.1:n.86C>G
ENST00000259455.3:c.476C>G ENSP00000259455.2:p.Thr159Ser
ENST00000477471.1:n.263C>G
ENST00000634227.1:n.250C>G
NM_005458.7:c.476C>G NP_005449.5:p.Thr159Ser
XM_017015331.2:c.182C>G XP_016870820.1:p.Thr61Ser
NM_005458.8:c.476C>G MANE Select NP_005449.5:p.Thr159Ser
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