Canonical Allele Identifier: CA2306830771
Gene: RAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59269142G= , CM000680.2:g.59269142G= GRCh38
NC_000018.9:g.56936374G= , CM000680.1:g.56936374G= GRCh37
NC_000018.8:g.55087354G= NCBI36
NG_013031.1:g.9252C=

Transcript Alleles

HGVS Amino-acid change
ENST00000334889.4:c.903C= MANE Select ENSP00000334813.3:p.Pro301=
ENST00000256852.7:c.*334C= ENSP00000256852.7:n.*334C=
ENST00000334889.3:c.903C= ENSP00000334813.3:p.Pro301=
NM_013435.2:c.903C= NP_038463.2:p.Pro301=
NM_013435.3:c.903C= MANE Select NP_038463.2:p.Pro301=