Canonical Allele Identifier: CA2674832893
Gene: WDR36 HGNC NCBI

Linked Data

gnomAD v4: 5-111119008-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119008T>C , CM000667.2:g.111119008T>C GRCh38
NC_000005.9:g.110454706T>C , CM000667.1:g.110454706T>C GRCh37
NC_000005.8:g.110482605T>C NCBI36
NG_008979.1:g.31837T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.1797-5T>C MANE Select ENSP00000424628.3:n.1797-5T>C
ENST00000506538.6:c.1965-5T>C ENSP00000423067.2:n.1965-5T>C
ENST00000513710.3:c.1797-5T>C ENSP00000424628.3:n.1797-5T>C
ENST00000612402.4:c.1965-5T>C ENSP00000479950.1:n.1965-5T>C
NM_139281.2:c.1965-5T>C NP_644810.1:n.1965-5T>C
XM_011543163.1:c.1965-5T>C XP_011541465.1:n.1965-5T>C
NM_139281.3:c.1797-5T>C MANE Select NP_644810.2:n.1797-5T>C
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