Canonical Allele Identifier: CA384637914
Gene: WNT1 HGNC NCBI

Linked Data

dbSNP Id: rs1941014147
MyVariant Identifiers: chr12:g.49375293T>G (hg19) chr12:g.48981510T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981510T>G , CM000674.2:g.48981510T>G GRCh38
NC_000012.11:g.49375293T>G , CM000674.1:g.49375293T>G GRCh37
NC_000012.10:g.47661560T>G NCBI36
NG_033141.1:g.8058T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.983T>G MANE Select ENSP00000293549.3:p.Leu328Arg
ENST00000293549.3:c.983T>G ENSP00000293549.3:p.Leu328Arg
ENST00000613114.4:c.950T>G ENSP00000481240.1:p.Leu317Arg
NM_005430.3:c.983T>G NP_005421.1:p.Leu328Arg
NM_005430.4:c.983T>G MANE Select NP_005421.1:p.Leu328Arg
Search 100 bp 5'
Search 100 bp 3'