Canonical Allele Identifier: CA561878359

Gene: WDR36

Linked Data

• dbSNP Id: rs1011819361
• gnomAD v2: 5-110433964-T-C
• gnomAD v3: 5-111098266-T-C
• gnomAD v4: 5-111098266-T-C
• MyVariant Identifiers: chr5:g.110433964T>C (hg19) ; chr5:g.111098266T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111098266T>C , CM000667.2:g.111098266T>C	GRCh38
NC_000005.9:g.110433964T>C , CM000667.1:g.110433964T>C	GRCh37
NC_000005.8:g.110461863T>C	NCBI36
NG_008979.1:g.11095T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.292-456T>C MANE Select	ENSP00000424628.3:n.292-456T>C
ENST00000504122.2:n.174-456T>C
ENST00000505303.5:n.428-456T>C
ENST00000506538.6:c.460-456T>C	ENSP00000423067.2:n.460-456T>C
ENST00000513710.3:c.292-456T>C	ENSP00000424628.3:n.292-456T>C
ENST00000612402.4:c.460-456T>C	ENSP00000479950.1:n.460-456T>C
NM_139281.2:c.460-456T>C	NP_644810.1:n.460-456T>C
XM_011543163.1:c.460-456T>C	XP_011541465.1:n.460-456T>C
NM_139281.3:c.292-456T>C MANE Select	NP_644810.2:n.292-456T>C