Canonical Allele Identifier: CA402583947
Gene: RAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59269137T>G , CM000680.2:g.59269137T>G GRCh38
NC_000018.9:g.56936369T>G , CM000680.1:g.56936369T>G GRCh37
NC_000018.8:g.55087349T>G NCBI36
NG_013031.1:g.9257A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000334889.4:c.908A>C MANE Select ENSP00000334813.3:p.Tyr303Ser
ENST00000256852.7:c.*339A>C ENSP00000256852.7:n.*339A>C
ENST00000334889.3:c.908A>C ENSP00000334813.3:p.Tyr303Ser
NM_013435.2:c.908A>C NP_038463.2:p.Tyr303Ser
NM_013435.3:c.908A>C MANE Select NP_038463.2:p.Tyr303Ser