Canonical Allele Identifier: CA1122156101

Gene:

Linked Data

• dbSNP Id: rs1823378926
• gnomAD v3: 9-21756068-CCTT-C
• gnomAD v4: 9-21756068-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21756072_21756074del , CM000671.2:g.21756072_21756074del	GRCh38
NC_000009.11:g.21756071_21756073del , CM000671.1:g.21756071_21756073del	GRCh37
NC_000009.10:g.21746071_21746073del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746563.2:n.163+11754_163+11756del