Canonical Allele Identifier: CA759294565

Gene:

Linked Data

• dbSNP Id: rs1292264038
• MyVariant Identifiers: chr2:g.156727242del (hg19) ; chr2:g.155870730del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.155870730del , CM000664.2:g.155870730del	GRCh38
NC_000002.11:g.156727242del , CM000664.1:g.156727242del	GRCh37
NC_000002.10:g.156435488del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923501.1:n.320-3543del
XR_001739749.1:n.331-29746del
XR_001739750.1:n.331-29746del
XR_001739751.1:n.331-29746del
XR_923501.2:n.331-3543del