Canonical Allele Identifier: CA2396046852
Gene: GNB1L HGNC NCBI

Linked Data

dbSNP Id: rs1937319517
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19797443C>A , CM000684.2:g.19797443C>A GRCh38
NC_000022.10:g.19784966C>A , CM000684.1:g.19784966C>A GRCh37
NC_000022.9:g.18164966C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000329517.11:c.732+4558G>T MANE Select ENSP00000331313.6:n.732+4558G>T
ENST00000329517.10:c.732+4558G>T ENSP00000331313.6:n.732+4558G>T
ENST00000403325.5:c.732+4558G>T ENSP00000385154.1:n.732+4558G>T
ENST00000405009.5:c.630+4660G>T ENSP00000384626.1:n.630+4660G>T
ENST00000460402.5:n.700+4558G>T
NM_053004.2:c.732+4558G>T NP_443730.1:n.732+4558G>T
NM_053004.3:c.732+4558G>T MANE Select NP_443730.1:n.732+4558G>T
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