Canonical Allele Identifier: CA3365890

Gene: WDR36

Linked Data

• dbSNP Id: rs763268664
• ExAC: 5:110454766 A / G
• gnomAD v2: 5-110454766-A-G
• MyVariant Identifiers: chr5:g.110454766A>G (hg19) ; chr5:g.111119068A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111119068A>G , CM000667.2:g.111119068A>G	GRCh38
NC_000005.9:g.110454766A>G , CM000667.1:g.110454766A>G	GRCh37
NC_000005.8:g.110482665A>G	NCBI36
NG_008979.1:g.31897A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1852A>G MANE Select	ENSP00000424628.3:p.Thr618Ala
ENST00000506538.6:c.2020A>G	ENSP00000423067.2:p.Thr674Ala
ENST00000513710.3:c.1852A>G	ENSP00000424628.3:p.Thr618Ala
ENST00000612402.4:c.2020A>G	ENSP00000479950.1:p.Thr674Ala
NM_139281.2:c.2020A>G	NP_644810.1:p.Thr674Ala
XM_011543163.1:c.2020A>G	XP_011541465.1:p.Thr674Ala
NM_139281.3:c.1852A>G MANE Select	NP_644810.2:p.Thr618Ala