Canonical Allele Identifier: CA504059311
Gene: RAX HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56939602G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59272370G>T , CM000680.2:g.59272370G>T GRCh38
NC_000018.9:g.56939602G>T , CM000680.1:g.56939602G>T GRCh37
NC_000018.8:g.55090582G>T NCBI36
NG_013031.1:g.6024C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000334889.4:c.534C>A MANE Select ENSP00000334813.3:p.Val178=
ENST00000256852.7:c.289+548C>A ENSP00000256852.7:n.289+548C>A
ENST00000334889.3:c.534C>A ENSP00000334813.3:p.Val178=
NM_013435.2:c.534C>A NP_038463.2:p.Val178=
NM_013435.3:c.534C>A MANE Select NP_038463.2:p.Val178=
Search 100 bp 5'
Search 100 bp 3'