Canonical Allele Identifier: CA95693500

Gene: ARAP2

Linked Data

• dbSNP Id: rs1044820133
• gnomAD v3: 4-35981514-T-C
• gnomAD v4: 4-35981514-T-C
• MyVariant Identifiers: chr4:g.35983136T>C (hg19) ; chr4:g.35981514T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.35981514T>C , CM000666.2:g.35981514T>C	GRCh38
NC_000004.11:g.35983136T>C , CM000666.1:g.35983136T>C	GRCh37
NC_000004.10:g.35659531T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503225.5:n.1607+3716A>G
XR_925192.1:n.1435A>G