Canonical Allele Identifier: CA354051621
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs201970872
gnomAD v2: 3-119133273-C-A
MyVariant Identifiers: chr3:g.119133273C>A (hg19) chr3:g.119414426C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414426C>A , CM000665.2:g.119414426C>A GRCh38
NC_000003.11:g.119133273C>A , CM000665.1:g.119133273C>A GRCh37
NC_000003.10:g.120615963C>A NCBI36
NG_007665.2:g.125054C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2497C>A MANE Select ENSP00000264245.4:p.Leu833Ile
ENST00000264245.8:c.2497C>A ENSP00000264245.4:p.Leu833Ile
NM_020754.3:c.2497C>A NP_065805.2:p.Leu833Ile
XM_005247671.3:c.2404C>A XP_005247728.1:p.Leu802Ile
XM_006713714.2:c.2437C>A XP_006713777.1:p.Leu813Ile
XM_006713714.3:c.2437C>A XP_006713777.1:p.Leu813Ile
XM_017006955.1:c.2005C>A XP_016862444.1:p.Leu669Ile
NM_020754.4:c.2497C>A MANE Select NP_065805.2:p.Leu833Ile
Search 100 bp 5'
Search 100 bp 3'