Canonical Allele Identifier: CA101277287
Gene: ARHGAP24 HGNC NCBI

Linked Data

dbSNP Id: rs927098976

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85752952T>G , CM000666.2:g.85752952T>G GRCh38
NC_000004.11:g.86674105T>G , CM000666.1:g.86674105T>G GRCh37
NC_000004.10:g.86893129T>G NCBI36
NG_051627.1:g.282822T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000395184.6:c.268+30980T>G MANE Select ENSP00000378611.1:n.268+30980T>G
ENST00000395184.5:c.268+30980T>G ENSP00000378611.1:n.268+30980T>G
ENST00000503995.5:c.268+30980T>G ENSP00000423206.1:n.268+30980T>G
ENST00000512201.5:c.-18+30980T>G ENSP00000426105.1:n.-18+30980T>G
NM_001025616.2:c.268+30980T>G NP_001020787.2:n.268+30980T>G
XM_005263263.3:c.268+30980T>G XP_005263320.1:n.268+30980T>G
XM_024454238.1:c.-18+30980T>G XP_024310006.1:n.-18+30980T>G
XM_024454239.1:c.-18+30980T>G XP_024310007.1:n.-18+30980T>G
NM_001025616.3:c.268+30980T>G MANE Select NP_001020787.2:n.268+30980T>G