Canonical Allele Identifier: CA11900158
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs4458523
gnomAD v2: 4-6289986-T-G
gnomAD v3: 4-6288259-T-G
gnomAD v4: 4-6288259-T-G
MyVariant Identifiers: chr4:g.6289986T>G (hg19) chr4:g.6288259T>G (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6288259T>G , CM000666.2:g.6288259T>G GRCh38
NC_000004.11:g.6289986T>G , CM000666.1:g.6289986T>G GRCh37
NC_000004.10:g.6340887T>G NCBI36
NG_011700.1:g.23410T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.316-728T>G ENSP00000507852.1:n.316-728T>G
ENST00000683395.1:c.306-728T>G
ENST00000684054.1:c.316-728T>G ENSP00000507120.1:n.316-728T>G
ENST00000684087.1:c.316-728T>G ENSP00000506978.1:n.316-728T>G
ENST00000684700.1:c.316-728T>G ENSP00000507806.1:n.316-728T>G
ENST00000506362.2:c.67-728T>G ENSP00000424103.2:n.67-728T>G
ENST00000673642.1:c.115-728T>G ENSP00000501242.1:n.115-728T>G
ENST00000673991.1:c.316-728T>G ENSP00000501033.1:n.316-728T>G
ENST00000674051.1:c.190-728T>G ENSP00000501083.1:n.190-728T>G
ENST00000226760.5:c.316-728T>G MANE Select ENSP00000226760.1:n.316-728T>G
ENST00000503569.5:c.316-728T>G ENSP00000423337.1:n.316-728T>G
NM_001145853.1:c.316-728T>G NP_001139325.1:n.316-728T>G
NM_006005.3:c.316-728T>G MANE Select NP_005996.2:n.316-728T>G
XM_017008586.1:c.325-728T>G XP_016864075.1:n.325-728T>G
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