Canonical Allele Identifier: CA1450583042
Gene: ARAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.35981395C= , CM000666.2:g.35981395C= GRCh38
NC_000004.11:g.35983017C= , CM000666.1:g.35983017C= GRCh37
NC_000004.10:g.35659412C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000503225.5:n.1607+3835G=
XR_925192.1:n.1554G=