Canonical Allele Identifier: CA2299236874
Gene: RIT2 HGNC NCBI

Linked Data

dbSNP Id: rs12456492
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.43093415A>T , CM000680.2:g.43093415A>T GRCh38
NC_000018.9:g.40673380A>T , CM000680.1:g.40673380A>T GRCh37
NC_000018.8:g.38927378A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326695.10:c.103+22002T>A MANE Select ENSP00000321805.4:n.103+22002T>A
ENST00000650392.1:c.103+22002T>A ENSP00000497708.1:n.103+22002T>A
ENST00000326695.9:c.103+22002T>A ENSP00000321805.4:n.103+22002T>A
ENST00000589109.5:c.103+22002T>A ENSP00000467217.1:n.103+22002T>A
ENST00000590910.1:c.103+22002T>A ENSP00000466620.1:n.103+22002T>A
NM_001272077.1:c.103+22002T>A NP_001259006.1:n.103+22002T>A
NM_002930.3:c.103+22002T>A NP_002921.1:n.103+22002T>A
NM_002930.4:c.103+22002T>A MANE Select NP_002921.1:n.103+22002T>A
NM_001272077.2:c.103+22002T>A NP_001259006.1:n.103+22002T>A
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