Canonical Allele Identifier: CA95693491

Gene: ARAP2

Linked Data

• dbSNP Id: rs1012911239
• gnomAD v2: 4-35983118-G-C
• gnomAD v3: 4-35981496-G-C
• gnomAD v4: 4-35981496-G-C
• MyVariant Identifiers: chr4:g.35983118G>C (hg19) ; chr4:g.35981496G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.35981496G>C , CM000666.2:g.35981496G>C	GRCh38
NC_000004.11:g.35983118G>C , CM000666.1:g.35983118G>C	GRCh37
NC_000004.10:g.35659513G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503225.5:n.1607+3734C>G
XR_925192.1:n.1453C>G