Canonical Allele Identifier: CA360613523
Gene: WDR36 HGNC NCBI

Linked Data

dbSNP Id: rs1451375525
gnomAD v2: 5-110454754-T-C
gnomAD v4: 5-111119056-T-C
MyVariant Identifiers: chr5:g.110454754T>C (hg19) chr5:g.111119056T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119056T>C , CM000667.2:g.111119056T>C GRCh38
NC_000005.9:g.110454754T>C , CM000667.1:g.110454754T>C GRCh37
NC_000005.8:g.110482653T>C NCBI36
NG_008979.1:g.31885T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1840T>C MANE Select ENSP00000424628.3:p.Ser614Pro
ENST00000506538.6:c.2008T>C ENSP00000423067.2:p.Ser670Pro
ENST00000513710.3:c.1840T>C ENSP00000424628.3:p.Ser614Pro
ENST00000612402.4:c.2008T>C ENSP00000479950.1:p.Ser670Pro
NM_139281.2:c.2008T>C NP_644810.1:p.Ser670Pro
XM_011543163.1:c.2008T>C XP_011541465.1:p.Ser670Pro
NM_139281.3:c.1840T>C MANE Select NP_644810.2:p.Ser614Pro
Search 100 bp 5'
Search 100 bp 3'