Canonical Allele Identifier: CA402584298
Gene: RAX HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56936458G>C (hg19) chr18:g.59269226G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59269226G>C , CM000680.2:g.59269226G>C GRCh38
NC_000018.9:g.56936458G>C , CM000680.1:g.56936458G>C GRCh37
NC_000018.8:g.55087438G>C NCBI36
NG_013031.1:g.9168C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000334889.4:c.819C>G MANE Select ENSP00000334813.3:p.Ser273Arg
ENST00000256852.7:c.*250C>G ENSP00000256852.7:n.*250C>G
ENST00000334889.3:c.819C>G ENSP00000334813.3:p.Ser273Arg
NM_013435.2:c.819C>G NP_038463.2:p.Ser273Arg
NM_013435.3:c.819C>G MANE Select NP_038463.2:p.Ser273Arg
Search 100 bp 5'
Search 100 bp 3'