Canonical Allele Identifier: CA124902667

Gene: WDR36

Linked Data

• dbSNP Id: rs762585058
• gnomAD v2: 5-110433965-C-G
• gnomAD v3: 5-111098267-C-G
• gnomAD v4: 5-111098267-C-G
• MyVariant Identifiers: chr5:g.110433965C>G (hg19) ; chr5:g.111098267C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111098267C>G , CM000667.2:g.111098267C>G	GRCh38
NC_000005.9:g.110433965C>G , CM000667.1:g.110433965C>G	GRCh37
NC_000005.8:g.110461864C>G	NCBI36
NG_008979.1:g.11096C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.292-455C>G MANE Select	ENSP00000424628.3:n.292-455C>G
ENST00000504122.2:n.174-455C>G
ENST00000505303.5:n.428-455C>G
ENST00000506538.6:c.460-455C>G	ENSP00000423067.2:n.460-455C>G
ENST00000513710.3:c.292-455C>G	ENSP00000424628.3:n.292-455C>G
ENST00000612402.4:c.460-455C>G	ENSP00000479950.1:n.460-455C>G
NM_139281.2:c.460-455C>G	NP_644810.1:n.460-455C>G
XM_011543163.1:c.460-455C>G	XP_011541465.1:n.460-455C>G
NM_139281.3:c.292-455C>G MANE Select	NP_644810.2:n.292-455C>G