Canonical Allele Identifier: CA797143966
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1256512042
MyVariant Identifiers: chr4:g.6271261C>T (hg19) chr4:g.6269534C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6269534C>T , CM000666.2:g.6269534C>T GRCh38
NC_000004.11:g.6271261C>T , CM000666.1:g.6271261C>T GRCh37
NC_000004.10:g.6322162C>T NCBI36
NG_011700.1:g.4685C>T

Transcript Alleles

HGVS Amino-acid change
XM_017008586.1:c.4+7895C>T XP_016864075.1:n.4+7895C>T
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