Canonical Allele Identifier: CA435411970
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119133170G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414323G>C , CM000665.2:g.119414323G>C GRCh38
NC_000003.11:g.119133170G>C , CM000665.1:g.119133170G>C GRCh37
NC_000003.10:g.120615860G>C NCBI36
NG_007665.2:g.124951G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2394G>C MANE Select ENSP00000264245.4:p.Leu798=
ENST00000264245.8:c.2394G>C ENSP00000264245.4:p.Leu798=
NM_020754.3:c.2394G>C NP_065805.2:p.Leu798=
XM_005247671.3:c.2301G>C XP_005247728.1:p.Leu767=
XM_006713714.2:c.2334G>C XP_006713777.1:p.Leu778=
XM_006713714.3:c.2334G>C XP_006713777.1:p.Leu778=
XM_017006955.1:c.1902G>C XP_016862444.1:p.Leu634=
NM_020754.4:c.2394G>C MANE Select NP_065805.2:p.Leu798=
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