Canonical Allele Identifier: CA95693483
Gene: ARAP2 HGNC NCBI

Linked Data

dbSNP Id: rs6834483
gnomAD v2: 4-35983111-C-T
gnomAD v3: 4-35981489-C-T
gnomAD v4: 4-35981489-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.35981489C>T , CM000666.2:g.35981489C>T GRCh38
NC_000004.11:g.35983111C>T , CM000666.1:g.35983111C>T GRCh37
NC_000004.10:g.35659506C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000503225.5:n.1607+3741G>A
XR_925192.1:n.1460G>A