Canonical Allele Identifier: CA2306830774
Gene: RAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59269143G= , CM000680.2:g.59269143G= GRCh38
NC_000018.9:g.56936375G= , CM000680.1:g.56936375G= GRCh37
NC_000018.8:g.55087355G= NCBI36
NG_013031.1:g.9251C=

Transcript Alleles

HGVS Amino-acid change
ENST00000334889.4:c.902C= MANE Select ENSP00000334813.3:p.Pro301=
ENST00000256852.7:c.*333C= ENSP00000256852.7:n.*333C=
ENST00000334889.3:c.902C= ENSP00000334813.3:p.Pro301=
NM_013435.2:c.902C= NP_038463.2:p.Pro301=
NM_013435.3:c.902C= MANE Select NP_038463.2:p.Pro301=