Canonical Allele Identifier: CA360613550

Gene: WDR36

Linked Data

• gnomAD v4: 5-111119069-C-T
• MyVariant Identifiers: chr5:g.110454767C>T (hg19) ; chr5:g.111119069C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111119069C>T , CM000667.2:g.111119069C>T	GRCh38
NC_000005.9:g.110454767C>T , CM000667.1:g.110454767C>T	GRCh37
NC_000005.8:g.110482666C>T	NCBI36
NG_008979.1:g.31898C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1853C>T MANE Select	ENSP00000424628.3:p.Thr618Ile
ENST00000506538.6:c.2021C>T	ENSP00000423067.2:p.Thr674Ile
ENST00000513710.3:c.1853C>T	ENSP00000424628.3:p.Thr618Ile
ENST00000612402.4:c.2021C>T	ENSP00000479950.1:p.Thr674Ile
NM_139281.2:c.2021C>T	NP_644810.1:p.Thr674Ile
XM_011543163.1:c.2021C>T	XP_011541465.1:p.Thr674Ile
NM_139281.3:c.1853C>T MANE Select	NP_644810.2:p.Thr618Ile