Canonical Allele Identifier: CA354051485
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs772306131
gnomAD v4: 3-119414404-A-C
MyVariant Identifiers: chr3:g.119133251A>C (hg19) chr3:g.119414404A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414404A>C , CM000665.2:g.119414404A>C GRCh38
NC_000003.11:g.119133251A>C , CM000665.1:g.119133251A>C GRCh37
NC_000003.10:g.120615941A>C NCBI36
NG_007665.2:g.125032A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2475A>C MANE Select ENSP00000264245.4:p.Gln825His
ENST00000264245.8:c.2475A>C ENSP00000264245.4:p.Gln825His
NM_020754.3:c.2475A>C NP_065805.2:p.Gln825His
XM_005247671.3:c.2382A>C XP_005247728.1:p.Gln794His
XM_006713714.2:c.2415A>C XP_006713777.1:p.Gln805His
XM_006713714.3:c.2415A>C XP_006713777.1:p.Gln805His
XM_017006955.1:c.1983A>C XP_016862444.1:p.Gln661His
NM_020754.4:c.2475A>C MANE Select NP_065805.2:p.Gln825His
Search 100 bp 5'
Search 100 bp 3'