Canonical Allele Identifier: CA95693527

Gene: ARAP2

Linked Data

• dbSNP Id: rs1006504797
• MyVariant Identifiers: chr4:g.35983152G>C (hg19) ; chr4:g.35981530G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.35981530G>C , CM000666.2:g.35981530G>C	GRCh38
NC_000004.11:g.35983152G>C , CM000666.1:g.35983152G>C	GRCh37
NC_000004.10:g.35659547G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000503225.5:n.1607+3700C>G
XR_925192.1:n.1419C>G