Canonical Allele Identifier: CA115072
Gene: WDR36 HGNC NCBI

Linked Data

ClinVar Variation Id: 1581
dbSNP Id: rs118204022

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111104342A>G , CM000667.2:g.111104342A>G GRCh38
NC_000005.9:g.110440041A>G , CM000667.1:g.110440041A>G GRCh37
NC_000005.8:g.110467940A>G NCBI36
NG_008979.1:g.17172A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.896A>G MANE Select ENSP00000424628.3:p.Asn299Ser
ENST00000505303.5:n.1032A>G
ENST00000506538.6:c.1064A>G ENSP00000423067.2:p.Asn355Ser
ENST00000513710.3:c.896A>G ENSP00000424628.3:p.Asn299Ser
ENST00000612402.4:c.1064A>G ENSP00000479950.1:p.Asn355Ser
NM_139281.2:c.1064A>G NP_644810.1:p.Asn355Ser
XM_011543163.1:c.1064A>G XP_011541465.1:p.Asn355Ser
NM_139281.3:c.896A>G MANE Select NP_644810.2:p.Asn299Ser