Canonical Allele Identifier: CA1061120801

Gene: ARAP2

Linked Data

• dbSNP Id: rs1306697517
• gnomAD v3: 4-35981393-T-C
• gnomAD v4: 4-35981393-T-C

Genomic Alleles

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

Transcript Alleles

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