Canonical Allele Identifier: CA1061120809
Gene: ARAP2 HGNC NCBI

Linked Data

dbSNP Id: rs1712076722
gnomAD v3: 4-35981429-T-A
gnomAD v4: 4-35981429-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.35981429T>A , CM000666.2:g.35981429T>A GRCh38
NC_000004.11:g.35983051T>A , CM000666.1:g.35983051T>A GRCh37
NC_000004.10:g.35659446T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000503225.5:n.1607+3801A>T
XR_925192.1:n.1520A>T
Search 100 bp 5'
Search 100 bp 3'