Canonical Allele Identifier: CA897778716
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs1332943071
MyVariant Identifiers: chr3:g.119132370A>T (hg19) chr3:g.119413523A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413523A>T , CM000665.2:g.119413523A>T GRCh38
NC_000003.11:g.119132370A>T , CM000665.1:g.119132370A>T GRCh37
NC_000003.10:g.120615060A>T NCBI36
NG_007665.2:g.124151A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.1927-333A>T MANE Select ENSP00000264245.4:n.1927-333A>T
ENST00000264245.8:c.1927-333A>T ENSP00000264245.4:n.1927-333A>T
NM_020754.3:c.1927-333A>T NP_065805.2:n.1927-333A>T
XM_005247671.3:c.1834-333A>T XP_005247728.1:n.1834-333A>T
XM_006713714.2:c.1867-333A>T XP_006713777.1:n.1867-333A>T
XM_006713714.3:c.1867-333A>T XP_006713777.1:n.1867-333A>T
XM_017006955.1:c.1435-333A>T XP_016862444.1:n.1435-333A>T
NM_020754.4:c.1927-333A>T MANE Select NP_065805.2:n.1927-333A>T
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