Canonical Allele Identifier: CA1450583049
Gene: ARAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.35981403G= , CM000666.2:g.35981403G= GRCh38
NC_000004.11:g.35983025G= , CM000666.1:g.35983025G= GRCh37
NC_000004.10:g.35659420G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000503225.5:n.1607+3827C=
XR_925192.1:n.1546C=