Canonical Allele Identifier: CA402583963
Gene: RAX HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000334889.4:c.904T>G MANE Select ENSP00000334813.3:p.Ser302Ala
ENST00000256852.7:c.*335T>G ENSP00000256852.7:n.*335T>G
ENST00000334889.3:c.904T>G ENSP00000334813.3:p.Ser302Ala
NM_013435.2:c.904T>G NP_038463.2:p.Ser302Ala
NM_013435.3:c.904T>G MANE Select NP_038463.2:p.Ser302Ala