Canonical Allele Identifier: CA550950238

Gene: ARAP2

Linked Data

• dbSNP Id: rs1484117239
• gnomAD v2: 4-35983054-G-C
• gnomAD v3: 4-35981432-G-C
• gnomAD v4: 4-35981432-G-C
• MyVariant Identifiers: chr4:g.35983054G>C (hg19) ; chr4:g.35981432G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.35981432G>C , CM000666.2:g.35981432G>C	GRCh38
NC_000004.11:g.35983054G>C , CM000666.1:g.35983054G>C	GRCh37
NC_000004.10:g.35659449G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503225.5:n.1607+3798C>G
XR_925192.1:n.1517C>G