Canonical Allele Identifier: CA729869727

Gene:

Linked Data

• dbSNP Id: rs1252886439
• gnomAD v3: 1-19874559-TC-T
• gnomAD v4: 1-19874559-TC-T
• MyVariant Identifiers: chr1:g.20201053del (hg19) ; chr1:g.19874560del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19874560del , CM000663.2:g.19874560del	GRCh38
NC_000001.10:g.20201053del , CM000663.1:g.20201053del	GRCh37
NC_000001.9:g.20073640del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_947027.1:n.266-8808del
XR_947028.1:n.266-8808del
XR_947027.2:n.167-8808del
XR_947028.2:n.167-8808del