Canonical Allele Identifier: CA7571545

Gene: WDR72

Linked Data

• ClinVar Variation Id: 316605
• ClinVar RCV Id: RCV000357408 ; RCV003389798
• dbSNP Id: rs148643501
• ExAC: 15:54025254 C / G
• gnomAD v2: 15-54025254-C-G
• gnomAD v3: 15-53733057-C-G
• gnomAD v4: 15-53733057-C-G
• MyVariant Identifiers: chr15:g.54025254C>G (hg19) ; chr15:g.53733057C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.53733057C>G , CM000677.2:g.53733057C>G	GRCh38
NC_000015.9:g.54025254C>G , CM000677.1:g.54025254C>G	GRCh37
NC_000015.8:g.51812546C>G	NCBI36
NG_017034.2:g.31606G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360509.10:c.93G>C MANE Select	ENSP00000353699.5:p.Thr31=
ENST00000360509.9:c.93G>C	ENSP00000353699.5:p.Thr31=
ENST00000396328.5:c.93G>C	ENSP00000379619.1:p.Thr31=
ENST00000557913.5:c.93G>C	ENSP00000453378.1:p.Thr31=
ENST00000559418.5:c.93G>C	ENSP00000452765.1:p.Thr31=
ENST00000560036.1:c.93G>C	ENSP00000453813.1:p.Thr31=
NM_182758.3:c.93G>C	NP_877435.3:p.Thr31=
NR_102334.1:n.333G>C
XM_011521433.1:c.93G>C	XP_011519735.1:p.Thr31=
XM_011521434.1:c.93G>C	XP_011519736.1:p.Thr31=
XM_011521435.1:c.93G>C	XP_011519737.1:p.Thr31=
XM_011521436.1:c.93G>C	XP_011519738.1:p.Thr31=
XM_011521437.1:c.93G>C	XP_011519739.1:p.Thr31=
XM_011521433.2:c.93G>C	XP_011519735.1:p.Thr31=
XM_011521435.2:c.93G>C	XP_011519737.1:p.Thr31=
XM_011521436.2:c.93G>C	XP_011519738.1:p.Thr31=
XM_011521437.2:c.93G>C	XP_011519739.1:p.Thr31=
XM_017022061.1:c.93G>C	XP_016877550.1:p.Thr31=
NM_182758.4:c.93G>C MANE Select	NP_877435.3:p.Thr31=
NR_102334.2:n.333G>C