Canonical Allele Identifier: CA360613567

Gene: WDR36

Linked Data

• MyVariant Identifiers: chr5:g.110454775T>G (hg19) ; chr5:g.111119077T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111119077T>G , CM000667.2:g.111119077T>G	GRCh38
NC_000005.9:g.110454775T>G , CM000667.1:g.110454775T>G	GRCh37
NC_000005.8:g.110482674T>G	NCBI36
NG_008979.1:g.31906T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1861T>G MANE Select	ENSP00000424628.3:p.Phe621Val
ENST00000506538.6:c.2029T>G	ENSP00000423067.2:p.Phe677Val
ENST00000513710.3:c.1861T>G	ENSP00000424628.3:p.Phe621Val
ENST00000612402.4:c.2029T>G	ENSP00000479950.1:p.Phe677Val
NM_139281.2:c.2029T>G	NP_644810.1:p.Phe677Val
XM_011543163.1:c.2029T>G	XP_011541465.1:p.Phe677Val
NM_139281.3:c.1861T>G MANE Select	NP_644810.2:p.Phe621Val