Canonical Allele Identifier: CA760016577

Gene:

Linked Data

• dbSNP Id: rs1157201495
• MyVariant Identifiers: chr2:g.16639323del (hg19) ; chr2:g.16458055del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.16458055del , CM000664.2:g.16458055del	GRCh38
NC_000002.11:g.16639323del , CM000664.1:g.16639323del	GRCh37
NC_000002.10:g.16502804del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_939752.1:n.396-2961del