Canonical Allele Identifier: CA95693494

Gene: ARAP2

Linked Data

• dbSNP Id: rs1052650370
• MyVariant Identifiers: chr4:g.35983134A>G (hg19) ; chr4:g.35981512A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.35981512A>G , CM000666.2:g.35981512A>G	GRCh38
NC_000004.11:g.35983134A>G , CM000666.1:g.35983134A>G	GRCh37
NC_000004.10:g.35659529A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503225.5:n.1607+3718T>C
XR_925192.1:n.1437T>C