Canonical Allele Identifier: CA322089851
Gene: GNB1L HGNC NCBI

Linked Data

dbSNP Id: rs967101681
MyVariant Identifiers: chr22:g.19784913A>G (hg19) chr22:g.19797390A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19797390A>G , CM000684.2:g.19797390A>G GRCh38
NC_000022.10:g.19784913A>G , CM000684.1:g.19784913A>G GRCh37
NC_000022.9:g.18164913A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000329517.11:c.732+4611T>C MANE Select ENSP00000331313.6:n.732+4611T>C
ENST00000329517.10:c.732+4611T>C ENSP00000331313.6:n.732+4611T>C
ENST00000403325.5:c.732+4611T>C ENSP00000385154.1:n.732+4611T>C
ENST00000405009.5:c.630+4713T>C ENSP00000384626.1:n.630+4713T>C
ENST00000460402.5:n.700+4611T>C
NM_053004.2:c.732+4611T>C NP_443730.1:n.732+4611T>C
NM_053004.3:c.732+4611T>C MANE Select NP_443730.1:n.732+4611T>C
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