Canonical Allele Identifier: CA350618267
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs1481386773
gnomAD v2: 2-219746936-A-G
gnomAD v3: 2-218882214-A-G
gnomAD v4: 2-218882214-A-G
MyVariant Identifiers: chr2:g.219746936A>G (hg19) chr2:g.218882214A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882214A>G , CM000664.2:g.218882214A>G GRCh38
NC_000002.11:g.219746936A>G , CM000664.1:g.219746936A>G GRCh37
NC_000002.10:g.219455180A>G NCBI36
NG_012179.1:g.6682A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.167A>G MANE Select ENSP00000258411.3:p.Asn56Ser
ENST00000258411.7:c.167A>G ENSP00000258411.3:p.Asn56Ser
ENST00000458582.1:c.54A>G
NM_025216.2:c.167A>G NP_079492.2:p.Asn56Ser
XM_011511928.1:c.116A>G XP_011510230.1:p.Asn39Ser
XM_011511929.1:c.71A>G XP_011510231.1:p.Asn24Ser
XM_011511930.1:c.167A>G XP_011510232.1:p.Asn56Ser
XM_011511929.2:c.71A>G XP_011510231.1:p.Asn24Ser
NM_025216.3:c.167A>G MANE Select NP_079492.2:p.Asn56Ser
Search 100 bp 5'
Search 100 bp 3'