Canonical Allele Identifier: CA95693465

Gene: ARAP2

Linked Data

• dbSNP Id: rs948509169
• gnomAD v3: 4-35981415-A-G
• gnomAD v4: 4-35981415-A-G
• MyVariant Identifiers: chr4:g.35983037A>G (hg19) ; chr4:g.35981415A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.35981415A>G , CM000666.2:g.35981415A>G	GRCh38
NC_000004.11:g.35983037A>G , CM000666.1:g.35983037A>G	GRCh37
NC_000004.10:g.35659432A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503225.5:n.1607+3815T>C
XR_925192.1:n.1534T>C