Canonical Allele Identifier: CA350618646
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219747003C>A (hg19) chr2:g.218882281C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882281C>A , CM000664.2:g.218882281C>A GRCh38
NC_000002.11:g.219747003C>A , CM000664.1:g.219747003C>A GRCh37
NC_000002.10:g.219455247C>A NCBI36
NG_012179.1:g.6749C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.234C>A MANE Select ENSP00000258411.3:p.His78Gln
ENST00000258411.7:c.234C>A ENSP00000258411.3:p.His78Gln
ENST00000458582.1:c.121C>A
NM_025216.2:c.234C>A NP_079492.2:p.His78Gln
XM_011511928.1:c.183C>A XP_011510230.1:p.His61Gln
XM_011511929.1:c.138C>A XP_011510231.1:p.His46Gln
XM_011511930.1:c.234C>A XP_011510232.1:p.His78Gln
XM_011511929.2:c.138C>A XP_011510231.1:p.His46Gln
NM_025216.3:c.234C>A MANE Select NP_079492.2:p.His78Gln
Search 100 bp 5'
Search 100 bp 3'