Canonical Allele Identifier: CA2554000
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs753595119
ExAC: 3:119133064 C / T
gnomAD v2: 3-119133064-C-T
gnomAD v4: 3-119414217-C-T
MyVariant Identifiers: chr3:g.119133064C>T (hg19) chr3:g.119414217C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414217C>T , CM000665.2:g.119414217C>T GRCh38
NC_000003.11:g.119133064C>T , CM000665.1:g.119133064C>T GRCh37
NC_000003.10:g.120615754C>T NCBI36
NG_007665.2:g.124845C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2288C>T MANE Select ENSP00000264245.4:p.Ala763Val
ENST00000264245.8:c.2288C>T ENSP00000264245.4:p.Ala763Val
NM_020754.3:c.2288C>T NP_065805.2:p.Ala763Val
XM_005247671.3:c.2195C>T XP_005247728.1:p.Ala732Val
XM_006713714.2:c.2228C>T XP_006713777.1:p.Ala743Val
XM_006713714.3:c.2228C>T XP_006713777.1:p.Ala743Val
XM_017006955.1:c.1796C>T XP_016862444.1:p.Ala599Val
NM_020754.4:c.2288C>T MANE Select NP_065805.2:p.Ala763Val
Search 100 bp 5'
Search 100 bp 3'