Canonical Allele Identifier: CA1033290640

Gene:

Linked Data

• dbSNP Id: rs1672668674
• gnomAD v3: 2-88015946-CCTCT-C
• gnomAD v4: 2-88015946-CCTCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88015949_88015952del , CM000664.2:g.88015949_88015952del	GRCh38
NC_000002.11:g.88315468_88315471del , CM000664.1:g.88315468_88315471del	GRCh37
NC_000002.10:g.88096583_88096586del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.294_297del
XR_940336.3:n.294_297del