Canonical Allele Identifier: CA402583951
Gene: RAX HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56936370A>G (hg19) chr18:g.59269138A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59269138A>G , CM000680.2:g.59269138A>G GRCh38
NC_000018.9:g.56936370A>G , CM000680.1:g.56936370A>G GRCh37
NC_000018.8:g.55087350A>G NCBI36
NG_013031.1:g.9256T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000334889.4:c.907T>C MANE Select ENSP00000334813.3:p.Tyr303His
ENST00000256852.7:c.*338T>C ENSP00000256852.7:n.*338T>C
ENST00000334889.3:c.907T>C ENSP00000334813.3:p.Tyr303His
NM_013435.2:c.907T>C NP_038463.2:p.Tyr303His
NM_013435.3:c.907T>C MANE Select NP_038463.2:p.Tyr303His
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