Canonical Allele Identifier: CA799419779
Gene: ARHGAP24 HGNC NCBI

Linked Data

dbSNP Id: rs1404645828
MyVariant Identifiers: chr4:g.86674333G>C (hg19) chr4:g.85753180G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85753180G>C , CM000666.2:g.85753180G>C GRCh38
NC_000004.11:g.86674333G>C , CM000666.1:g.86674333G>C GRCh37
NC_000004.10:g.86893357G>C NCBI36
NG_051627.1:g.283050G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000395184.6:c.268+31208G>C MANE Select ENSP00000378611.1:n.268+31208G>C
ENST00000395184.5:c.268+31208G>C ENSP00000378611.1:n.268+31208G>C
ENST00000503995.5:c.268+31208G>C ENSP00000423206.1:n.268+31208G>C
ENST00000512201.5:c.-18+31208G>C ENSP00000426105.1:n.-18+31208G>C
NM_001025616.2:c.268+31208G>C NP_001020787.2:n.268+31208G>C
XM_005263263.3:c.268+31208G>C XP_005263320.1:n.268+31208G>C
XM_024454238.1:c.-18+31208G>C XP_024310006.1:n.-18+31208G>C
XM_024454239.1:c.-18+31208G>C XP_024310007.1:n.-18+31208G>C
NM_001025616.3:c.268+31208G>C MANE Select NP_001020787.2:n.268+31208G>C
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