Canonical Allele Identifier: CA679994587
Gene: ARAP1 HGNC NCBI

Linked Data

dbSNP Id: rs1430834580
MyVariant Identifiers: chr11:g.72433539G>C (hg19) chr11:g.72722494G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722494G>C , CM000673.2:g.72722494G>C GRCh38
NC_000011.9:g.72433539G>C , CM000673.1:g.72433539G>C GRCh37
NC_000011.8:g.72111187G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393609.8:c.509+4126C>G MANE Select ENSP00000377233.3:n.509+4126C>G
ENST00000359373.9:c.509+4126C>G ENSP00000352332.5:n.509+4126C>G
ENST00000393609.7:c.509+4126C>G ENSP00000377233.3:n.509+4126C>G
NM_001040118.2:c.509+4126C>G NP_001035207.1:n.509+4126C>G
NM_001040118.3:c.509+4126C>G MANE Select NP_001035207.1:n.509+4126C>G
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