Canonical Allele Identifier: CA894254453

Gene:

Linked Data

• dbSNP Id: rs1459506528
• MyVariant Identifiers: chr2:g.88315782_88315794del (hg19) ; chr2:g.88016263_88016275del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016264_88016276del , CM000664.2:g.88016264_88016276del	GRCh38
NC_000002.11:g.88315783_88315795del , CM000664.1:g.88315783_88315795del	GRCh37
NC_000002.10:g.88096898_88096910del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.609_621del
XR_940336.3:n.609_621del