Canonical Allele Identifier: CA91777128

Gene: WFS1

Linked Data

• dbSNP Id: rs1026156216
• MyVariant Identifiers: chr4:g.6271141G>C (hg19) ; chr4:g.6269414G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6269414G>C , CM000666.2:g.6269414G>C	GRCh38
NC_000004.11:g.6271141G>C , CM000666.1:g.6271141G>C	GRCh37
NC_000004.10:g.6322042G>C	NCBI36
NG_011700.1:g.4565G>C

Transcript Alleles

HGVS	Amino-acid change
XM_017008586.1:c.4+7775G>C	XP_016864075.1:n.4+7775G>C