Canonical Allele Identifier: CA2396046780
Gene: GNB1L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19797300T= , CM000684.2:g.19797300T= GRCh38
NC_000022.10:g.19784823T= , CM000684.1:g.19784823T= GRCh37
NC_000022.9:g.18164823T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000329517.11:c.732+4701A= MANE Select ENSP00000331313.6:n.732+4701A=
ENST00000329517.10:c.732+4701A= ENSP00000331313.6:n.732+4701A=
ENST00000403325.5:c.732+4701A= ENSP00000385154.1:n.732+4701A=
ENST00000405009.5:c.630+4803A= ENSP00000384626.1:n.630+4803A=
ENST00000460402.5:n.700+4701A=
NM_053004.2:c.732+4701A= NP_443730.1:n.732+4701A=
NM_053004.3:c.732+4701A= MANE Select NP_443730.1:n.732+4701A=
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