Canonical Allele Identifier: CA751455554
Gene: GNB1L HGNC NCBI

Linked Data

dbSNP Id: rs1410473844
MyVariant Identifiers: chr22:g.19785120C>T (hg19) chr22:g.19797597C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19797597C>T , CM000684.2:g.19797597C>T GRCh38
NC_000022.10:g.19785120C>T , CM000684.1:g.19785120C>T GRCh37
NC_000022.9:g.18165120C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000329517.11:c.732+4404G>A MANE Select ENSP00000331313.6:n.732+4404G>A
ENST00000329517.10:c.732+4404G>A ENSP00000331313.6:n.732+4404G>A
ENST00000403325.5:c.732+4404G>A ENSP00000385154.1:n.732+4404G>A
ENST00000405009.5:c.630+4506G>A ENSP00000384626.1:n.630+4506G>A
ENST00000460402.5:n.700+4404G>A
NM_053004.2:c.732+4404G>A NP_443730.1:n.732+4404G>A
NM_053004.3:c.732+4404G>A MANE Select NP_443730.1:n.732+4404G>A
Search 100 bp 5'
Search 100 bp 3'