Canonical Allele Identifier: CA354051639
Gene: ARHGAP31 HGNC NCBI

Linked Data

gnomAD v4: 3-119414430-G-C
MyVariant Identifiers: chr3:g.119133277G>C (hg19) chr3:g.119414430G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414430G>C , CM000665.2:g.119414430G>C GRCh38
NC_000003.11:g.119133277G>C , CM000665.1:g.119133277G>C GRCh37
NC_000003.10:g.120615967G>C NCBI36
NG_007665.2:g.125058G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2501G>C MANE Select ENSP00000264245.4:p.Cys834Ser
ENST00000264245.8:c.2501G>C ENSP00000264245.4:p.Cys834Ser
NM_020754.3:c.2501G>C NP_065805.2:p.Cys834Ser
XM_005247671.3:c.2408G>C XP_005247728.1:p.Cys803Ser
XM_006713714.2:c.2441G>C XP_006713777.1:p.Cys814Ser
XM_006713714.3:c.2441G>C XP_006713777.1:p.Cys814Ser
XM_017006955.1:c.2009G>C XP_016862444.1:p.Cys670Ser
NM_020754.4:c.2501G>C MANE Select NP_065805.2:p.Cys834Ser
Search 100 bp 5'
Search 100 bp 3'