Canonical Allele Identifier: CA905231271

Gene:

Linked Data

• dbSNP Id: rs1282004529
• gnomAD v3: 3-21207134-AT-A
• gnomAD v4: 3-21207134-AT-A
• MyVariant Identifiers: chr3:g.21248627del (hg19) ; chr3:g.21207135del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.21207137del , CM000665.2:g.21207137del	GRCh38
NC_000003.11:g.21248629del , CM000665.1:g.21248629del	GRCh37
NC_000003.10:g.21223633del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940646.1:n.254-3861del
XR_940646.2:n.547-3861del