Canonical Allele Identifier: CA2306830679
Gene: RAX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59269065G= , CM000680.2:g.59269065G= GRCh38
NC_000018.9:g.56936297G= , CM000680.1:g.56936297G= GRCh37
NC_000018.8:g.55087277G= NCBI36
NG_013031.1:g.9329C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334889.4:c.980C= MANE Select ENSP00000334813.3:p.Ala327=
ENST00000256852.7:c.*411C= ENSP00000256852.7:n.*411C=
ENST00000334889.3:c.980C= ENSP00000334813.3:p.Ala327=
NM_013435.2:c.980C= NP_038463.2:p.Ala327=
NM_013435.3:c.980C= MANE Select NP_038463.2:p.Ala327=
Search 100 bp 5'
Search 100 bp 3'