Canonical Allele Identifier: CA338916603
Gene: WNT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.22446857G>T (hg19) chr1:g.22120364G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22120364G>T , CM000663.2:g.22120364G>T GRCh38
NC_000001.10:g.22446857G>T , CM000663.1:g.22446857G>T GRCh37
NC_000001.9:g.22319444G>T NCBI36
NG_008974.1:g.27663C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000290167.11:c.742C>A MANE Select ENSP00000290167.5:p.Arg248Ser
ENST00000290167.10:c.742C>A ENSP00000290167.5:p.Arg248Ser
NM_030761.4:c.742C>A NP_110388.2:p.Arg248Ser
XM_011541597.1:c.808C>A XP_011539899.1:p.Arg270Ser
XM_011541598.1:c.577C>A XP_011539900.1:p.Arg193Ser
XM_011541597.2:c.808C>A XP_011539899.1:p.Arg270Ser
XM_011541598.2:c.577C>A XP_011539900.1:p.Arg193Ser
NM_030761.5:c.742C>A MANE Select NP_110388.2:p.Arg248Ser
Search 100 bp 5'
Search 100 bp 3'