Canonical Allele Identifier: CA100990903
Gene: RASGEF1B HGNC NCBI

Linked Data

dbSNP Id: rs931287275
gnomAD v2: 4-82462609-G-C
gnomAD v3: 4-81541455-G-C
gnomAD v4: 4-81541455-G-C
MyVariant Identifiers: chr4:g.82462609G>C (hg19) chr4:g.81541455G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.81541455G>C , CM000666.2:g.81541455G>C GRCh38
NC_000004.11:g.82462609G>C , CM000666.1:g.82462609G>C GRCh37
NC_000004.10:g.82681633G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638048.1:c.255+61384C>G ENSP00000490436.1:n.255+61384C>G
ENST00000512716.1:c.-140-19910C>G ENSP00000476065.1:n.-140-19910C>G
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