Canonical Allele Identifier: CA2737946355
Gene: GNB1L HGNC NCBI

Linked Data

dbSNP Id: rs2145864183
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19797577A>G , CM000684.2:g.19797577A>G GRCh38
NC_000022.10:g.19785100A>G , CM000684.1:g.19785100A>G GRCh37
NC_000022.9:g.18165100A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000329517.11:c.732+4424T>C MANE Select ENSP00000331313.6:n.732+4424T>C
ENST00000329517.10:c.732+4424T>C ENSP00000331313.6:n.732+4424T>C
ENST00000403325.5:c.732+4424T>C ENSP00000385154.1:n.732+4424T>C
ENST00000405009.5:c.630+4526T>C ENSP00000384626.1:n.630+4526T>C
ENST00000460402.5:n.700+4424T>C
NM_053004.2:c.732+4424T>C NP_443730.1:n.732+4424T>C
NM_053004.3:c.732+4424T>C MANE Select NP_443730.1:n.732+4424T>C
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