Canonical Allele Identifier: CA1450583094
Gene: ARAP2 HGNC NCBI

Linked Data

dbSNP Id: rs1712077145

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.35981452A>G , CM000666.2:g.35981452A>G GRCh38
NC_000004.11:g.35983074A>G , CM000666.1:g.35983074A>G GRCh37
NC_000004.10:g.35659469A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000503225.5:n.1607+3778T>C
XR_925192.1:n.1497T>C