Canonical Allele Identifier: CA360613646
Gene: WDR36 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110454811T>G (hg19) chr5:g.111119113T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119113T>G , CM000667.2:g.111119113T>G GRCh38
NC_000005.9:g.110454811T>G , CM000667.1:g.110454811T>G GRCh37
NC_000005.8:g.110482710T>G NCBI36
NG_008979.1:g.31942T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1897T>G MANE Select ENSP00000424628.3:p.Tyr633Asp
ENST00000506538.6:c.2065T>G ENSP00000423067.2:p.Tyr689Asp
ENST00000513710.3:c.1897T>G ENSP00000424628.3:p.Tyr633Asp
ENST00000612402.4:c.2065T>G ENSP00000479950.1:p.Tyr689Asp
NM_139281.2:c.2065T>G NP_644810.1:p.Tyr689Asp
XM_011543163.1:c.2065T>G XP_011541465.1:p.Tyr689Asp
NM_139281.3:c.1897T>G MANE Select NP_644810.2:p.Tyr633Asp
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