Canonical Allele Identifier: CA2396046821
Gene: GNB1L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19797360C= , CM000684.2:g.19797360C= GRCh38
NC_000022.10:g.19784883C= , CM000684.1:g.19784883C= GRCh37
NC_000022.9:g.18164883C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000329517.11:c.732+4641G= MANE Select ENSP00000331313.6:n.732+4641G=
ENST00000329517.10:c.732+4641G= ENSP00000331313.6:n.732+4641G=
ENST00000403325.5:c.732+4641G= ENSP00000385154.1:n.732+4641G=
ENST00000405009.5:c.630+4743G= ENSP00000384626.1:n.630+4743G=
ENST00000460402.5:n.700+4641G=
NM_053004.2:c.732+4641G= NP_443730.1:n.732+4641G=
NM_053004.3:c.732+4641G= MANE Select NP_443730.1:n.732+4641G=
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