Canonical Allele Identifier: CA1064685980
Gene: RASGEF1B HGNC NCBI

Linked Data

dbSNP Id: rs1724165333
gnomAD v3: 4-81541453-T-C
gnomAD v4: 4-81541453-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.81541453T>C , CM000666.2:g.81541453T>C GRCh38
NC_000004.11:g.82462607T>C , CM000666.1:g.82462607T>C GRCh37
NC_000004.10:g.82681631T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638048.1:c.255+61386A>G ENSP00000490436.1:n.255+61386A>G
ENST00000512716.1:c.-140-19908A>G ENSP00000476065.1:n.-140-19908A>G
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