Canonical Allele Identifier: CA969917756
Gene: WDR72 HGNC NCBI

Linked Data

dbSNP Id: rs2015208959

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.53650802A>G , CM000677.2:g.53650802A>G GRCh38
NC_000015.9:g.53942999A>G , CM000677.1:g.53942999A>G GRCh37
NC_000015.8:g.51730291A>G NCBI36
NG_017034.2:g.113861T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360509.10:c.1962+14770T>C MANE Select ENSP00000353699.5:n.1962+14770T>C
ENST00000360509.9:c.1962+14770T>C ENSP00000353699.5:n.1962+14770T>C
ENST00000396328.5:c.1962+14770T>C ENSP00000379619.1:n.1962+14770T>C
ENST00000557913.5:c.1953+14770T>C ENSP00000453378.1:n.1953+14770T>C
ENST00000559418.5:c.1992+14770T>C ENSP00000452765.1:n.1992+14770T>C
ENST00000560036.1:c.1962+14770T>C ENSP00000453813.1:n.1962+14770T>C
NM_182758.3:c.1962+14770T>C NP_877435.3:n.1962+14770T>C
NR_102334.1:n.2202+14770T>C
XM_011521433.1:c.1962+14770T>C XP_011519735.1:n.1962+14770T>C
XM_011521434.1:c.1962+14770T>C XP_011519736.1:n.1962+14770T>C
XM_011521435.1:c.1962+14770T>C XP_011519737.1:n.1962+14770T>C
XM_011521436.1:c.1944+14770T>C XP_011519738.1:n.1944+14770T>C
XM_011521437.1:c.1842+14770T>C XP_011519739.1:n.1842+14770T>C
XM_011521433.2:c.1962+14770T>C XP_011519735.1:n.1962+14770T>C
XM_011521435.2:c.1962+14770T>C XP_011519737.1:n.1962+14770T>C
XM_011521436.2:c.1944+14770T>C XP_011519738.1:n.1944+14770T>C
XM_011521437.2:c.1842+14770T>C XP_011519739.1:n.1842+14770T>C
XM_017022061.1:c.1962+14770T>C XP_016877550.1:n.1962+14770T>C
NM_182758.4:c.1962+14770T>C MANE Select NP_877435.3:n.1962+14770T>C
NR_102334.2:n.2202+14770T>C