Canonical Allele Identifier: CA1450583083
Gene: ARAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.35981446A= , CM000666.2:g.35981446A= GRCh38
NC_000004.11:g.35983068A= , CM000666.1:g.35983068A= GRCh37
NC_000004.10:g.35659463A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000503225.5:n.1607+3784T=
XR_925192.1:n.1503T=