Canonical Allele Identifier: CA2554043
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs755464720
ExAC: 3:119133231 A / T
gnomAD v2: 3-119133231-A-T
gnomAD v3: 3-119414384-A-T
gnomAD v4: 3-119414384-A-T
MyVariant Identifiers: chr3:g.119133231A>T (hg19) chr3:g.119414384A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414384A>T , CM000665.2:g.119414384A>T GRCh38
NC_000003.11:g.119133231A>T , CM000665.1:g.119133231A>T GRCh37
NC_000003.10:g.120615921A>T NCBI36
NG_007665.2:g.125012A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2455A>T MANE Select ENSP00000264245.4:p.Ile819Leu
ENST00000264245.8:c.2455A>T ENSP00000264245.4:p.Ile819Leu
NM_020754.3:c.2455A>T NP_065805.2:p.Ile819Leu
XM_005247671.3:c.2362A>T XP_005247728.1:p.Ile788Leu
XM_006713714.2:c.2395A>T XP_006713777.1:p.Ile799Leu
XM_006713714.3:c.2395A>T XP_006713777.1:p.Ile799Leu
XM_017006955.1:c.1963A>T XP_016862444.1:p.Ile655Leu
NM_020754.4:c.2455A>T MANE Select NP_065805.2:p.Ile819Leu
Search 100 bp 5'
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