Canonical Allele Identifier: CA1450583079
Gene: ARAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.35981437T= , CM000666.2:g.35981437T= GRCh38
NC_000004.11:g.35983059T= , CM000666.1:g.35983059T= GRCh37
NC_000004.10:g.35659454T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000503225.5:n.1607+3793A=
XR_925192.1:n.1512A=