Canonical Allele Identifier: CA794406369

Gene: ARAP2

Linked Data

• dbSNP Id: rs1306697517
• gnomAD v3: 4-35981393-T-A
• gnomAD v4: 4-35981393-T-A
• MyVariant Identifiers: chr4:g.35983015T>A (hg19) ; chr4:g.35981393T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.35981393T>A , CM000666.2:g.35981393T>A	GRCh38
NC_000004.11:g.35983015T>A , CM000666.1:g.35983015T>A	GRCh37
NC_000004.10:g.35659410T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503225.5:n.1607+3837A>T
XR_925192.1:n.1556A>T