Canonical Allele Identifier: CA354049604
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs2080744231
MyVariant Identifiers: chr3:g.119132951G>C (hg19) chr3:g.119414104G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414104G>C , CM000665.2:g.119414104G>C GRCh38
NC_000003.11:g.119132951G>C , CM000665.1:g.119132951G>C GRCh37
NC_000003.10:g.120615641G>C NCBI36
NG_007665.2:g.124732G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2175G>C MANE Select ENSP00000264245.4:p.Gln725His
ENST00000264245.8:c.2175G>C ENSP00000264245.4:p.Gln725His
NM_020754.3:c.2175G>C NP_065805.2:p.Gln725His
XM_005247671.3:c.2082G>C XP_005247728.1:p.Gln694His
XM_006713714.2:c.2115G>C XP_006713777.1:p.Gln705His
XM_006713714.3:c.2115G>C XP_006713777.1:p.Gln705His
XM_017006955.1:c.1683G>C XP_016862444.1:p.Gln561His
NM_020754.4:c.2175G>C MANE Select NP_065805.2:p.Gln725His
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