Canonical Allele Identifier: CA1033291603

Gene:

Linked Data

• dbSNP Id: rs1672685547
• gnomAD v3: 2-88016351-GTT-G
• gnomAD v4: 2-88016351-GTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016352_88016353del , CM000664.2:g.88016352_88016353del	GRCh38
NC_000002.11:g.88315871_88315872del , CM000664.1:g.88315871_88315872del	GRCh37
NC_000002.10:g.88096986_88096987del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.697_698del
XR_940336.3:n.697_698del