Canonical Allele Identifier: CA794406380

Gene: ARAP2

Linked Data

• dbSNP Id: rs1292159896
• gnomAD v3: 4-35981426-T-C
• gnomAD v4: 4-35981426-T-C
• MyVariant Identifiers: chr4:g.35983048T>C (hg19) ; chr4:g.35981426T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.35981426T>C , CM000666.2:g.35981426T>C	GRCh38
NC_000004.11:g.35983048T>C , CM000666.1:g.35983048T>C	GRCh37
NC_000004.10:g.35659443T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503225.5:n.1607+3804A>G
XR_925192.1:n.1523A>G