Canonical Allele Identifier: CA1866994002
Gene: GABBR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541749G= , CM000671.2:g.98541749G= GRCh38
NC_000009.11:g.101304031G= , CM000671.1:g.101304031G= GRCh37
NC_000009.10:g.100343852G= NCBI36
NG_016426.1:g.172449C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.630+124C= MANE Select ENSP00000259455.2:n.630+124C=
ENST00000637410.1:n.408+124C=
ENST00000259455.3:c.630+124C= ENSP00000259455.2:n.630+124C=
ENST00000477471.1:n.417+124C=
ENST00000634227.1:n.404+124C=
NM_005458.7:c.630+124C= NP_005449.5:n.630+124C=
XM_017015331.2:c.336+124C= XP_016870820.1:n.336+124C=
NM_005458.8:c.630+124C= MANE Select NP_005449.5:n.630+124C=
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