Canonical Allele Identifier: CA756214934

Gene:

Linked Data

• dbSNP Id: rs1275980720
• MyVariant Identifiers: chr2:g.123641532del (hg19) ; chr2:g.122883956del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122883956del , CM000664.2:g.122883956del	GRCh38
NC_000002.11:g.123641532del , CM000664.1:g.123641532del	GRCh37
NC_000002.10:g.123358002del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923292.1:n.1125-986del
XR_001739692.1:n.1451-986del
XR_923292.2:n.1358-986del