Canonical Allele Identifier: CA2113839
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs774127616
ExAC: 2:219746911 C / T
gnomAD v2: 2-219746911-C-T
gnomAD v3: 2-218882189-C-T
gnomAD v4: 2-218882189-C-T
MyVariant Identifiers: chr2:g.219746911C>T (hg19) chr2:g.218882189C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882189C>T , CM000664.2:g.218882189C>T GRCh38
NC_000002.11:g.219746911C>T , CM000664.1:g.219746911C>T GRCh37
NC_000002.10:g.219455155C>T NCBI36
NG_012179.1:g.6657C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.142C>T MANE Select ENSP00000258411.3:p.Arg48Cys
ENST00000258411.7:c.142C>T ENSP00000258411.3:p.Arg48Cys
ENST00000458582.1:c.29C>T
NM_025216.2:c.142C>T NP_079492.2:p.Arg48Cys
XM_011511928.1:c.91C>T XP_011510230.1:p.Arg31Cys
XM_011511929.1:c.46C>T XP_011510231.1:p.Arg16Cys
XM_011511930.1:c.142C>T XP_011510232.1:p.Arg48Cys
XM_011511929.2:c.46C>T XP_011510231.1:p.Arg16Cys
NM_025216.3:c.142C>T MANE Select NP_079492.2:p.Arg48Cys
Search 100 bp 5'
Search 100 bp 3'