Canonical Allele Identifier: CA350586997
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219754984G>C (hg19) chr2:g.218890262G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218890262G>C , CM000664.2:g.218890262G>C GRCh38
NC_000002.11:g.219754984G>C , CM000664.1:g.219754984G>C GRCh37
NC_000002.10:g.219463228G>C NCBI36
NG_012179.1:g.14730G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.655G>C MANE Select ENSP00000258411.3:p.Gly219Arg
ENST00000258411.7:c.655G>C ENSP00000258411.3:p.Gly219Arg
ENST00000458582.1:c.264-2512G>C
NM_025216.2:c.655G>C NP_079492.2:p.Gly219Arg
XM_011511928.1:c.604G>C XP_011510230.1:p.Gly202Arg
XM_011511929.1:c.559G>C XP_011510231.1:p.Gly187Arg
XM_011511930.1:c.377-2512G>C XP_011510232.1:n.377-2512G>C
XM_011511929.2:c.559G>C XP_011510231.1:p.Gly187Arg
NM_025216.3:c.655G>C MANE Select NP_079492.2:p.Gly219Arg
Search 100 bp 5'
Search 100 bp 3'