Canonical Allele Identifier: CA360613628
Gene: WDR36 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110454803T>A (hg19) chr5:g.111119105T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119105T>A , CM000667.2:g.111119105T>A GRCh38
NC_000005.9:g.110454803T>A , CM000667.1:g.110454803T>A GRCh37
NC_000005.8:g.110482702T>A NCBI36
NG_008979.1:g.31934T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1889T>A MANE Select ENSP00000424628.3:p.Leu630His
ENST00000506538.6:c.2057T>A ENSP00000423067.2:p.Leu686His
ENST00000513710.3:c.1889T>A ENSP00000424628.3:p.Leu630His
ENST00000612402.4:c.2057T>A ENSP00000479950.1:p.Leu686His
NM_139281.2:c.2057T>A NP_644810.1:p.Leu686His
XM_011543163.1:c.2057T>A XP_011541465.1:p.Leu686His
NM_139281.3:c.1889T>A MANE Select NP_644810.2:p.Leu630His
Search 100 bp 5'
Search 100 bp 3'