Canonical Allele Identifier: CA402583857
Gene: RAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59269118G>T , CM000680.2:g.59269118G>T GRCh38
NC_000018.9:g.56936350G>T , CM000680.1:g.56936350G>T GRCh37
NC_000018.8:g.55087330G>T NCBI36
NG_013031.1:g.9276C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334889.4:c.927C>A MANE Select ENSP00000334813.3:p.Phe309Leu
ENST00000256852.7:c.*358C>A ENSP00000256852.7:n.*358C>A
ENST00000334889.3:c.927C>A ENSP00000334813.3:p.Phe309Leu
NM_013435.2:c.927C>A NP_038463.2:p.Phe309Leu
NM_013435.3:c.927C>A MANE Select NP_038463.2:p.Phe309Leu