Canonical Allele Identifier: CA717005219
Gene: IQGAP1 HGNC NCBI

Linked Data

dbSNP Id: rs1221225787
gnomAD v3: 15-90500978-T-C
gnomAD v4: 15-90500978-T-C
MyVariant Identifiers: chr15:g.91044210T>C (hg19) chr15:g.90500978T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90500978T>C , CM000677.2:g.90500978T>C GRCh38
NC_000015.9:g.91044210T>C , CM000677.1:g.91044210T>C GRCh37
NC_000015.8:g.88845214T>C NCBI36
NG_052946.1:g.117738T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000268182.10:c.*870T>C MANE Select ENSP00000268182.5:n.*870T>C
ENST00000268182.9:c.*870T>C ENSP00000268182.5:n.*870T>C
ENST00000558957.1:n.1902T>C
ENST00000561086.1:n.1611T>C
NM_003870.3:c.*870T>C NP_003861.1:n.*870T>C
XR_001751409.2:n.5973T>C
NM_003870.4:c.*870T>C MANE Select NP_003861.1:n.*870T>C
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