Canonical Allele Identifier: CA3365884

Gene: WDR36

Linked Data

• ClinVar Variation Id: 1366550
• ClinVar RCV Id: RCV001962088
• dbSNP Id: rs772011041
• ExAC: 5:110454737 C / T
• gnomAD v2: 5-110454737-C-T
• gnomAD v3: 5-111119039-C-T
• gnomAD v4: 5-111119039-C-T
• MyVariant Identifiers: chr5:g.110454737C>T (hg19) ; chr5:g.111119039C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111119039C>T , CM000667.2:g.111119039C>T	GRCh38
NC_000005.9:g.110454737C>T , CM000667.1:g.110454737C>T	GRCh37
NC_000005.8:g.110482636C>T	NCBI36
NG_008979.1:g.31868C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000513710.4:c.1823C>T MANE Select	ENSP00000424628.3:p.Ser608Leu
ENST00000506538.6:c.1991C>T	ENSP00000423067.2:p.Ser664Leu
ENST00000513710.3:c.1823C>T	ENSP00000424628.3:p.Ser608Leu
ENST00000612402.4:c.1991C>T	ENSP00000479950.1:p.Ser664Leu
NM_139281.2:c.1991C>T	NP_644810.1:p.Ser664Leu
XM_011543163.1:c.1991C>T	XP_011541465.1:p.Ser664Leu
NM_139281.3:c.1823C>T MANE Select	NP_644810.2:p.Ser608Leu