Canonical Allele Identifier: CA402583673

Gene: RAX

Linked Data

• MyVariant Identifiers: chr18:g.56936309C>G (hg19) ; chr18:g.59269077C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59269077C>G , CM000680.2:g.59269077C>G	GRCh38
NC_000018.9:g.56936309C>G , CM000680.1:g.56936309C>G	GRCh37
NC_000018.8:g.55087289C>G	NCBI36
NG_013031.1:g.9317G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334889.4:c.968G>C MANE Select	ENSP00000334813.3:p.Ser323Thr
ENST00000256852.7:c.*399G>C	ENSP00000256852.7:n.*399G>C
ENST00000334889.3:c.968G>C	ENSP00000334813.3:p.Ser323Thr
NM_013435.2:c.968G>C	NP_038463.2:p.Ser323Thr
NM_013435.3:c.968G>C MANE Select	NP_038463.2:p.Ser323Thr