Canonical Allele Identifier: CA619561917
Gene: IQGAP1 HGNC NCBI

Linked Data

dbSNP Id: rs1333178389
gnomAD v2: 15-91044382-A-G
gnomAD v3: 15-90501150-A-G
gnomAD v4: 15-90501150-A-G
COSMIC: COSN1181897
MyVariant Identifiers: chr15:g.91044382A>G (hg19) chr15:g.90501150A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90501150A>G , CM000677.2:g.90501150A>G GRCh38
NC_000015.9:g.91044382A>G , CM000677.1:g.91044382A>G GRCh37
NC_000015.8:g.88845386A>G NCBI36
NG_052946.1:g.117910A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000268182.10:c.*1042A>G MANE Select ENSP00000268182.5:n.*1042A>G
ENST00000268182.9:c.*1042A>G ENSP00000268182.5:n.*1042A>G
ENST00000558957.1:n.2074A>G
ENST00000561086.1:n.1783A>G
NM_003870.3:c.*1042A>G NP_003861.1:n.*1042A>G
XR_001751409.2:n.6145A>G
NM_003870.4:c.*1042A>G MANE Select NP_003861.1:n.*1042A>G
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