Canonical Allele Identifier: CA550950246

Gene: ARAP2

Linked Data

• dbSNP Id: rs1379673407
• gnomAD v2: 4-35983135-G-A
• MyVariant Identifiers: chr4:g.35983135G>A (hg19) ; chr4:g.35981513G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.35981513G>A , CM000666.2:g.35981513G>A	GRCh38
NC_000004.11:g.35983135G>A , CM000666.1:g.35983135G>A	GRCh37
NC_000004.10:g.35659530G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503225.5:n.1607+3717C>T
XR_925192.1:n.1436C>T