Canonical Allele Identifier: CA2306830769
Gene: RAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59269141A= , CM000680.2:g.59269141A= GRCh38
NC_000018.9:g.56936373A= , CM000680.1:g.56936373A= GRCh37
NC_000018.8:g.55087353A= NCBI36
NG_013031.1:g.9253T=

Transcript Alleles

HGVS Amino-acid change
ENST00000334889.4:c.904T= MANE Select ENSP00000334813.3:p.Ser302=
ENST00000256852.7:c.*335T= ENSP00000256852.7:n.*335T=
ENST00000334889.3:c.904T= ENSP00000334813.3:p.Ser302=
NM_013435.2:c.904T= NP_038463.2:p.Ser302=
NM_013435.3:c.904T= MANE Select NP_038463.2:p.Ser302=