Canonical Allele Identifier: CA360613584
Gene: WDR36 HGNC NCBI

Linked Data

dbSNP Id: rs1315447932
gnomAD v2: 5-110454782-C-T
gnomAD v4: 5-111119084-C-T
MyVariant Identifiers: chr5:g.110454782C>T (hg19) chr5:g.111119084C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119084C>T , CM000667.2:g.111119084C>T GRCh38
NC_000005.9:g.110454782C>T , CM000667.1:g.110454782C>T GRCh37
NC_000005.8:g.110482681C>T NCBI36
NG_008979.1:g.31913C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1868C>T MANE Select ENSP00000424628.3:p.Ala623Val
ENST00000506538.6:c.2036C>T ENSP00000423067.2:p.Ala679Val
ENST00000513710.3:c.1868C>T ENSP00000424628.3:p.Ala623Val
ENST00000612402.4:c.2036C>T ENSP00000479950.1:p.Ala679Val
NM_139281.2:c.2036C>T NP_644810.1:p.Ala679Val
XM_011543163.1:c.2036C>T XP_011541465.1:p.Ala679Val
NM_139281.3:c.1868C>T MANE Select NP_644810.2:p.Ala623Val
Search 100 bp 5'
Search 100 bp 3'