Canonical Allele Identifier: CA1021127353

Gene:

Linked Data

• dbSNP Id: rs1981482773
• gnomAD v3: 21-22259402-TG-T
• gnomAD v4: 21-22259402-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.22259403del , CM000683.2:g.22259403del	GRCh38
NC_000021.8:g.23631723del , CM000683.1:g.23631723del	GRCh37
NC_000021.7:g.22553594del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001754978.1:n.221+46590del