Canonical Allele Identifier: CA124932961
Gene: WDR36 HGNC NCBI

Linked Data

dbSNP Id: rs1013367136
gnomAD v2: 5-110454991-A-G
gnomAD v3: 5-111119293-A-G
gnomAD v4: 5-111119293-A-G
MyVariant Identifiers: chr5:g.110454991A>G (hg19) chr5:g.111119293A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119293A>G , CM000667.2:g.111119293A>G GRCh38
NC_000005.9:g.110454991A>G , CM000667.1:g.110454991A>G GRCh37
NC_000005.8:g.110482890A>G NCBI36
NG_008979.1:g.32122A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1904+173A>G MANE Select ENSP00000424628.3:n.1904+173A>G
ENST00000506538.6:c.2072+173A>G ENSP00000423067.2:n.2072+173A>G
ENST00000513710.3:c.1904+173A>G ENSP00000424628.3:n.1904+173A>G
ENST00000612402.4:c.2072+173A>G ENSP00000479950.1:n.2072+173A>G
NM_139281.2:c.2072+173A>G NP_644810.1:n.2072+173A>G
XM_011543163.1:c.2072+173A>G XP_011541465.1:n.2072+173A>G
NM_139281.3:c.1904+173A>G MANE Select NP_644810.2:n.1904+173A>G
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