Canonical Allele Identifier: CA2322939
Gene: WDR48 HGNC NCBI

Linked Data

ClinVar Variation Id: 424665
dbSNP Id: rs148407227
gnomAD v2: 3-39108050-T-G
gnomAD v3: 3-39066559-T-G
gnomAD v4: 3-39066559-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39066559T>G , CM000665.2:g.39066559T>G GRCh38
NC_000003.11:g.39108050T>G , CM000665.1:g.39108050T>G GRCh37
NC_000003.10:g.39083054T>G NCBI36
NG_051663.1:g.19574T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302313.10:c.280T>G MANE Select ENSP00000307491.5:p.Ser94Ala
ENST00000302313.9:c.280T>G ENSP00000307491.5:p.Ser94Ala
ENST00000413099.6:c.*9T>G ENSP00000388720.2:n.*9T>G
ENST00000420940.6:c.280T>G ENSP00000415963.2:p.Ser94Ala
ENST00000423296.6:c.280T>G ENSP00000401421.2:p.Ser94Ala
ENST00000433841.6:c.*75T>G ENSP00000406025.2:n.*75T>G
ENST00000441361.1:c.70T>G ENSP00000416900.1:p.Ser24Ala
NM_001303402.1:c.34T>G NP_001290331.1:p.Ser12Ala
NM_001303403.1:c.269-16T>G NP_001290332.1:n.269-16T>G
NM_020839.3:c.280T>G NP_065890.1:p.Ser94Ala
XM_005265346.2:c.280T>G XP_005265403.1:p.Ser94Ala
XM_011533971.1:c.70T>G XP_011532273.1:p.Ser24Ala
XR_940485.1:n.310T>G
NM_001346225.1:c.280T>G NP_001333154.1:p.Ser94Ala
NM_001346226.1:c.109T>G NP_001333155.1:p.Ser37Ala
NM_001346227.1:c.-116T>G NP_001333156.1:n.-116T>G
NM_001346228.1:c.70T>G NP_001333157.1:p.Ser24Ala
NR_144399.1:n.320T>G
NR_144400.1:n.320T>G
NR_144401.1:n.320T>G
XM_005265346.4:c.280T>G XP_005265403.1:p.Ser94Ala
XM_011533971.2:c.70T>G XP_011532273.1:p.Ser24Ala
NM_020839.4:c.280T>G MANE Select NP_065890.1:p.Ser94Ala
NM_001303402.2:c.34T>G NP_001290331.1:p.Ser12Ala
NM_001303403.2:c.269-16T>G NP_001290332.1:n.269-16T>G
NM_001346225.2:c.280T>G NP_001333154.1:p.Ser94Ala
NM_001346226.2:c.109T>G NP_001333155.1:p.Ser37Ala
NM_001346227.2:c.-116T>G NP_001333156.1:n.-116T>G
NR_144399.2:n.290T>G
NR_144400.2:n.290T>G
NR_144401.2:n.290T>G
NM_001346228.2:c.70T>G NP_001333157.1:p.Ser24Ala