Canonical Allele Identifier: CA91776996
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs866354285
MyVariant Identifiers: chr4:g.6270994A>G (hg19) chr4:g.6269267A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269267A>G , CM000666.2:g.6269267A>G GRCh38
NC_000004.11:g.6270994A>G , CM000666.1:g.6270994A>G GRCh37
NC_000004.10:g.6321895A>G NCBI36
NG_011700.1:g.4418A>G

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7628A>G XP_016864075.1:n.4+7628A>G
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