Canonical Allele Identifier: CA2396046854

Gene: GNB1L

Linked Data

• dbSNP Id: rs1937319556

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19797450A>G , CM000684.2:g.19797450A>G	GRCh38
NC_000022.10:g.19784973A>G , CM000684.1:g.19784973A>G	GRCh37
NC_000022.9:g.18164973A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000329517.11:c.732+4551T>C MANE Select	ENSP00000331313.6:n.732+4551T>C
ENST00000329517.10:c.732+4551T>C	ENSP00000331313.6:n.732+4551T>C
ENST00000403325.5:c.732+4551T>C	ENSP00000385154.1:n.732+4551T>C
ENST00000405009.5:c.630+4653T>C	ENSP00000384626.1:n.630+4653T>C
ENST00000460402.5:n.700+4551T>C
NM_053004.2:c.732+4551T>C	NP_443730.1:n.732+4551T>C
NM_053004.3:c.732+4551T>C MANE Select	NP_443730.1:n.732+4551T>C