Canonical Allele Identifier: CA402583959
Gene: RAX HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56936372G>T (hg19) chr18:g.59269140G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59269140G>T , CM000680.2:g.59269140G>T GRCh38
NC_000018.9:g.56936372G>T , CM000680.1:g.56936372G>T GRCh37
NC_000018.8:g.55087352G>T NCBI36
NG_013031.1:g.9254C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000334889.4:c.905C>A MANE Select ENSP00000334813.3:p.Ser302Tyr
ENST00000256852.7:c.*336C>A ENSP00000256852.7:n.*336C>A
ENST00000334889.3:c.905C>A ENSP00000334813.3:p.Ser302Tyr
NM_013435.2:c.905C>A NP_038463.2:p.Ser302Tyr
NM_013435.3:c.905C>A MANE Select NP_038463.2:p.Ser302Tyr
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