Canonical Allele Identifier: CA500649581
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.44851098G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773732G>T , CM000679.2:g.46773732G>T GRCh38
NC_000017.10:g.44851098G>T , CM000679.1:g.44851098G>T GRCh37
NC_000017.9:g.42206261G>T NCBI36
NG_008084.2:g.49985C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.63C>A (WNT3) ENSP00000516418.1:p.Gly21=
ENST00000225512.6:c.258C>A (WNT3) MANE Select ENSP00000225512.5:p.Gly86=
ENST00000225512.5:c.258C>A (WNT3) ENSP00000225512.5:p.Gly86=
NM_030753.4:c.258C>A (WNT3) NP_110380.1:p.Gly86=
XM_024450773.1:c.4809+223213G>T (LRRC37A2) XP_024306541.1:n.4809+223213G>T
NM_030753.5:c.258C>A (WNT3) MANE Select NP_110380.1:p.Gly86=
Search 100 bp 5'
Search 100 bp 3'