Canonical Allele Identifier: CA445744825
Gene: WDR36 HGNC NCBI

Linked Data

gnomAD v4: 5-111119043-T-A
MyVariant Identifiers: chr5:g.110454741T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119043T>A , CM000667.2:g.111119043T>A GRCh38
NC_000005.9:g.110454741T>A , CM000667.1:g.110454741T>A GRCh37
NC_000005.8:g.110482640T>A NCBI36
NG_008979.1:g.31872T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1827T>A MANE Select ENSP00000424628.3:p.Ala609=
ENST00000506538.6:c.1995T>A ENSP00000423067.2:p.Ala665=
ENST00000513710.3:c.1827T>A ENSP00000424628.3:p.Ala609=
ENST00000612402.4:c.1995T>A ENSP00000479950.1:p.Ala665=
NM_139281.2:c.1995T>A NP_644810.1:p.Ala665=
XM_011543163.1:c.1995T>A XP_011541465.1:p.Ala665=
NM_139281.3:c.1827T>A MANE Select NP_644810.2:p.Ala609=
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