Canonical Allele Identifier: CA95693515

Gene: ARAP2

Linked Data

• dbSNP Id: rs1030956703
• gnomAD v3: 4-35981523-G-A
• gnomAD v4: 4-35981523-G-A
• MyVariant Identifiers: chr4:g.35983145G>A (hg19) ; chr4:g.35981523G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.35981523G>A , CM000666.2:g.35981523G>A	GRCh38
NC_000004.11:g.35983145G>A , CM000666.1:g.35983145G>A	GRCh37
NC_000004.10:g.35659540G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503225.5:n.1607+3707C>T
XR_925192.1:n.1426C>T