Canonical Allele Identifier: CA15177496
Gene: WNT10A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10177996

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218881839T>C , CM000664.2:g.218881839T>C GRCh38
NC_000002.10:g.219454805T>C NCBI36
NC_000002.11:g.219746561T>C , CM000664.1:g.219746561T>C GRCh37
NG_012179.1:g.6307T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.7:c.114-322T>C ENSP00000258411.3:p.=
NM_025216.2:c.114-322T>C NP_079492.2:p.=
XM_011511928.1:c.63-322T>C XP_011510230.1:p.=
XM_011511929.1:c.18-322T>C XP_011510231.1:p.=
XM_011511930.1:c.114-322T>C XP_011510232.1:p.=