Canonical Allele Identifier: CA779464749
Gene: RIT2 HGNC NCBI

Linked Data

dbSNP Id: rs1357777594
MyVariant Identifiers: chr18:g.40678278C>G (hg19) chr18:g.43098313C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.43098313C>G , CM000680.2:g.43098313C>G GRCh38
NC_000018.9:g.40678278C>G , CM000680.1:g.40678278C>G GRCh37
NC_000018.8:g.38932276C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326695.10:c.103+17104G>C MANE Select ENSP00000321805.4:n.103+17104G>C
ENST00000650392.1:c.103+17104G>C ENSP00000497708.1:n.103+17104G>C
ENST00000326695.9:c.103+17104G>C ENSP00000321805.4:n.103+17104G>C
ENST00000589109.5:c.103+17104G>C ENSP00000467217.1:n.103+17104G>C
ENST00000590910.1:c.103+17104G>C ENSP00000466620.1:n.103+17104G>C
NM_001272077.1:c.103+17104G>C NP_001259006.1:n.103+17104G>C
NM_002930.3:c.103+17104G>C NP_002921.1:n.103+17104G>C
NM_002930.4:c.103+17104G>C MANE Select NP_002921.1:n.103+17104G>C
NM_001272077.2:c.103+17104G>C NP_001259006.1:n.103+17104G>C
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