Canonical Allele Identifier: CA402583523

Gene: RAX

Linked Data

• MyVariant Identifiers: chr18:g.56936273T>G (hg19) ; chr18:g.59269041T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59269041T>G , CM000680.2:g.59269041T>G	GRCh38
NC_000018.9:g.56936273T>G , CM000680.1:g.56936273T>G	GRCh37
NC_000018.8:g.55087253T>G	NCBI36
NG_013031.1:g.9353A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334889.4:c.1004A>C MANE Select	ENSP00000334813.3:p.His335Pro
ENST00000256852.7:c.*435A>C	ENSP00000256852.7:n.*435A>C
ENST00000334889.3:c.1004A>C	ENSP00000334813.3:p.His335Pro
NM_013435.2:c.1004A>C	NP_038463.2:p.His335Pro
NM_013435.3:c.1004A>C MANE Select	NP_038463.2:p.His335Pro