Canonical Allele Identifier: CA2809671924
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46788165C>T , CM000679.2:g.46788165C>T GRCh38
NC_000017.10:g.44865531C>T , CM000679.1:g.44865531C>T GRCh37
NC_000017.9:g.42220691C>T NCBI36
NG_008084.2:g.35552G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-115-14256G>A (WNT3) ENSP00000516418.1:n.-115-14256G>A
ENST00000225512.6:c.81-14256G>A (WNT3) MANE Select ENSP00000225512.5:n.81-14256G>A
ENST00000225512.5:c.81-14256G>A (WNT3) ENSP00000225512.5:n.81-14256G>A
ENST00000573788.5:n.492-14256G>A (WNT3)
NM_030753.4:c.81-14256G>A (WNT3) NP_110380.1:n.81-14256G>A
XM_024450773.1:c.4809+237646C>T (LRRC37A2) XP_024306541.1:n.4809+237646C>T
NM_030753.5:c.81-14256G>A (WNT3) MANE Select NP_110380.1:n.81-14256G>A
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