Canonical Allele Identifier: CA2113862
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 464180
ClinVar RCV Id: RCV000558141 RCV001829581
dbSNP Id: rs373607885
ExAC: 2:219746985 G / T
gnomAD v2: 2-219746985-G-T
gnomAD v3: 2-218882263-G-T
gnomAD v4: 2-218882263-G-T
MyVariant Identifiers: chr2:g.219746985G>T (hg19) chr2:g.218882263G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882263G>T , CM000664.2:g.218882263G>T GRCh38
NC_000002.11:g.219746985G>T , CM000664.1:g.219746985G>T GRCh37
NC_000002.10:g.219455229G>T NCBI36
NG_012179.1:g.6731G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.216G>T MANE Select ENSP00000258411.3:p.Met72Ile
ENST00000258411.7:c.216G>T ENSP00000258411.3:p.Met72Ile
ENST00000458582.1:c.103G>T
NM_025216.2:c.216G>T NP_079492.2:p.Met72Ile
XM_011511928.1:c.165G>T XP_011510230.1:p.Met55Ile
XM_011511929.1:c.120G>T XP_011510231.1:p.Met40Ile
XM_011511930.1:c.216G>T XP_011510232.1:p.Met72Ile
XM_011511929.2:c.120G>T XP_011510231.1:p.Met40Ile
NM_025216.3:c.216G>T MANE Select NP_079492.2:p.Met72Ile
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Search 100 bp 3'