Canonical Allele Identifier: CA2306830777
Gene: RAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59269146G= , CM000680.2:g.59269146G= GRCh38
NC_000018.9:g.56936378G= , CM000680.1:g.56936378G= GRCh37
NC_000018.8:g.55087358G= NCBI36
NG_013031.1:g.9248C=

Transcript Alleles

HGVS Amino-acid change
ENST00000334889.4:c.899C= MANE Select ENSP00000334813.3:p.Pro300=
ENST00000256852.7:c.*330C= ENSP00000256852.7:n.*330C=
ENST00000334889.3:c.899C= ENSP00000334813.3:p.Pro300=
NM_013435.2:c.899C= NP_038463.2:p.Pro300=
NM_013435.3:c.899C= MANE Select NP_038463.2:p.Pro300=