Canonical Allele Identifier: CA2737946295
Gene: GNB1L HGNC NCBI

Linked Data

dbSNP Id: rs2145864051
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19797404_19797405del , CM000684.2:g.19797404_19797405del GRCh38
NC_000022.10:g.19784927_19784928del , CM000684.1:g.19784927_19784928del GRCh37
NC_000022.9:g.18164927_18164928del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000329517.11:c.732+4596_732+4597del MANE Select ENSP00000331313.6:n.732+4596_732+4597del
ENST00000329517.10:c.732+4596_732+4597del ENSP00000331313.6:n.732+4596_732+4597del
ENST00000403325.5:c.732+4596_732+4597del ENSP00000385154.1:n.732+4596_732+4597del
ENST00000405009.5:c.630+4698_630+4699del ENSP00000384626.1:n.630+4698_630+4699del
ENST00000460402.5:n.700+4596_700+4597del
NM_053004.2:c.732+4596_732+4597del NP_443730.1:n.732+4596_732+4597del
NM_053004.3:c.732+4596_732+4597del MANE Select NP_443730.1:n.732+4596_732+4597del
Search 100 bp 5'
Search 100 bp 3'