Canonical Allele Identifier: CA2396046874

Gene: GNB1L

Linked Data

• dbSNP Id: rs1937320183

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19797489_19797490del , CM000684.2:g.19797489_19797490del	GRCh38
NC_000022.10:g.19785012_19785013del , CM000684.1:g.19785012_19785013del	GRCh37
NC_000022.9:g.18165012_18165013del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000329517.11:c.732+4515_732+4516del MANE Select	ENSP00000331313.6:n.732+4515_732+4516del
ENST00000329517.10:c.732+4515_732+4516del	ENSP00000331313.6:n.732+4515_732+4516del
ENST00000403325.5:c.732+4515_732+4516del	ENSP00000385154.1:n.732+4515_732+4516del
ENST00000405009.5:c.630+4617_630+4618del	ENSP00000384626.1:n.630+4617_630+4618del
ENST00000460402.5:n.700+4515_700+4516del
NM_053004.2:c.732+4515_732+4516del	NP_443730.1:n.732+4515_732+4516del
NM_053004.3:c.732+4515_732+4516del MANE Select	NP_443730.1:n.732+4515_732+4516del