Canonical Allele Identifier: CA1450583082
Gene: ARAP2 HGNC NCBI

Linked Data

dbSNP Id: rs1712076970

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.35981445_35981446del , CM000666.2:g.35981445_35981446del GRCh38
NC_000004.11:g.35983067_35983068del , CM000666.1:g.35983067_35983068del GRCh37
NC_000004.10:g.35659462_35659463del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000503225.5:n.1607+3785_1607+3786del
XR_925192.1:n.1504_1505del