Canonical Allele Identifier: CA2299126096
Gene: RIT2 HGNC NCBI

Linked Data

dbSNP Id: rs1907222553
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42857692C>A , CM000680.2:g.42857692C>A GRCh38
NC_000018.9:g.40437657C>A , CM000680.1:g.40437657C>A GRCh37
NC_000018.8:g.38691655C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326695.10:c.426+65880G>T MANE Select ENSP00000321805.4:n.426+65880G>T
ENST00000650392.1:c.*56-12523G>T ENSP00000497708.1:n.*56-12523G>T
ENST00000326695.9:c.426+65880G>T ENSP00000321805.4:n.426+65880G>T
ENST00000589109.5:c.*28+63005G>T ENSP00000467217.1:n.*28+63005G>T
ENST00000590910.1:c.488+65880G>T ENSP00000466620.1:n.488+65880G>T
NM_001272077.1:c.*28+63005G>T NP_001259006.1:n.*28+63005G>T
NM_002930.3:c.426+65880G>T NP_002921.1:n.426+65880G>T
NM_002930.4:c.426+65880G>T MANE Select NP_002921.1:n.426+65880G>T
NM_001272077.2:c.*28+63005G>T NP_001259006.1:n.*28+63005G>T
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