Canonical Allele Identifier: CA897778765
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs1284008963
gnomAD v3: 3-119413682-T-G
gnomAD v4: 3-119413682-T-G
MyVariant Identifiers: chr3:g.119132529T>G (hg19) chr3:g.119413682T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413682T>G , CM000665.2:g.119413682T>G GRCh38
NC_000003.11:g.119132529T>G , CM000665.1:g.119132529T>G GRCh37
NC_000003.10:g.120615219T>G NCBI36
NG_007665.2:g.124310T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.1927-174T>G MANE Select ENSP00000264245.4:n.1927-174T>G
ENST00000264245.8:c.1927-174T>G ENSP00000264245.4:n.1927-174T>G
NM_020754.3:c.1927-174T>G NP_065805.2:n.1927-174T>G
XM_005247671.3:c.1834-174T>G XP_005247728.1:n.1834-174T>G
XM_006713714.2:c.1867-174T>G XP_006713777.1:n.1867-174T>G
XM_006713714.3:c.1867-174T>G XP_006713777.1:n.1867-174T>G
XM_017006955.1:c.1435-174T>G XP_016862444.1:n.1435-174T>G
NM_020754.4:c.1927-174T>G MANE Select NP_065805.2:n.1927-174T>G
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