Canonical Allele Identifier: CA729869677

Gene:

Linked Data

• dbSNP Id: rs1235078174
• MyVariant Identifiers: chr1:g.20200926_20200947del (hg19) ; chr1:g.19874433_19874454del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19874433_19874454del , CM000663.2:g.19874433_19874454del	GRCh38
NC_000001.10:g.20200926_20200947del , CM000663.1:g.20200926_20200947del	GRCh37
NC_000001.9:g.20073513_20073534del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_947027.1:n.266-8702_266-8681del
XR_947028.1:n.266-8702_266-8681del
XR_947027.2:n.167-8702_167-8681del
XR_947028.2:n.167-8702_167-8681del