Canonical Allele Identifier: CA1061120826
Gene: ARAP2 HGNC NCBI

Linked Data

dbSNP Id: rs1712078106
gnomAD v3: 4-35981497-T-C
gnomAD v4: 4-35981497-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.35981497T>C , CM000666.2:g.35981497T>C GRCh38
NC_000004.11:g.35983119T>C , CM000666.1:g.35983119T>C GRCh37
NC_000004.10:g.35659514T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000503225.5:n.1607+3733A>G
XR_925192.1:n.1452A>G
Search 100 bp 5'
Search 100 bp 3'