Canonical Allele Identifier: CA206716569
Gene: RASGEF1A HGNC NCBI

Linked Data

dbSNP Id: rs28461806
gnomAD v2: 10-43755754-T-C
gnomAD v3: 10-43260306-T-C
gnomAD v4: 10-43260306-T-C
MyVariant Identifiers: chr10:g.43755754T>C (hg19) chr10:g.43260306T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43260306T>C , CM000672.2:g.43260306T>C GRCh38
NC_000010.10:g.43755754T>C , CM000672.1:g.43755754T>C GRCh37
NC_000010.9:g.43075760T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000395810.6:c.-7+6539A>G MANE Select ENSP00000379155.1:n.-7+6539A>G
ENST00000395810.5:c.-7+6539A>G ENSP00000379155.1:n.-7+6539A>G
NM_145313.3:c.-7+6539A>G NP_660356.2:n.-7+6539A>G
NM_145313.4:c.-7+6539A>G MANE Select NP_660356.2:n.-7+6539A>G
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