Canonical Allele Identifier: CA801872679
Gene: WDR36 HGNC NCBI

Linked Data

dbSNP Id: rs1227150247
MyVariant Identifiers: chr5:g.110434058G>A (hg19) chr5:g.111098360G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111098360G>A , CM000667.2:g.111098360G>A GRCh38
NC_000005.9:g.110434058G>A , CM000667.1:g.110434058G>A GRCh37
NC_000005.8:g.110461957G>A NCBI36
NG_008979.1:g.11189G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.292-362G>A MANE Select ENSP00000424628.3:n.292-362G>A
ENST00000504122.2:n.174-362G>A
ENST00000505303.5:n.428-362G>A
ENST00000506538.6:c.460-362G>A ENSP00000423067.2:n.460-362G>A
ENST00000513710.3:c.292-362G>A ENSP00000424628.3:n.292-362G>A
ENST00000612402.4:c.460-362G>A ENSP00000479950.1:n.460-362G>A
NM_139281.2:c.460-362G>A NP_644810.1:n.460-362G>A
XM_011543163.1:c.460-362G>A XP_011541465.1:n.460-362G>A
NM_139281.3:c.292-362G>A MANE Select NP_644810.2:n.292-362G>A
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