Canonical Allele Identifier: CA2638676316

Gene:

Linked Data

• gnomAD v4: 17-50211824-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50211826del , CM000679.2:g.50211826del	GRCh38
NC_000017.10:g.48289187del , CM000679.1:g.48289187del	GRCh37
NC_000017.9:g.45644186del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_934838.1:n.43-2009del