Canonical Allele Identifier: CA350618292
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219746941A>C (hg19) chr2:g.218882219A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882219A>C , CM000664.2:g.218882219A>C GRCh38
NC_000002.11:g.219746941A>C , CM000664.1:g.219746941A>C GRCh37
NC_000002.10:g.219455185A>C NCBI36
NG_012179.1:g.6687A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.172A>C MANE Select ENSP00000258411.3:p.Asn58His
ENST00000258411.7:c.172A>C ENSP00000258411.3:p.Asn58His
ENST00000458582.1:c.59A>C
NM_025216.2:c.172A>C NP_079492.2:p.Asn58His
XM_011511928.1:c.121A>C XP_011510230.1:p.Asn41His
XM_011511929.1:c.76A>C XP_011510231.1:p.Asn26His
XM_011511930.1:c.172A>C XP_011510232.1:p.Asn58His
XM_011511929.2:c.76A>C XP_011510231.1:p.Asn26His
NM_025216.3:c.172A>C MANE Select NP_079492.2:p.Asn58His
Search 100 bp 5'
Search 100 bp 3'