Canonical Allele Identifier: CA10641910
Gene: RAX HGNC NCBI

Linked Data

ClinVar Variation Id: 327525
ClinVar RCV Id: RCV000310452
dbSNP Id: rs3744893
gnomAD v2: 18-56935860-G-A
gnomAD v3: 18-59268628-G-A
gnomAD v4: 18-59268628-G-A
MyVariant Identifiers: chr18:g.56935860G>A (hg19) chr18:g.59268628G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59268628G>A , CM000680.2:g.59268628G>A GRCh38
NC_000018.9:g.56935860G>A , CM000680.1:g.56935860G>A GRCh37
NC_000018.8:g.55086840G>A NCBI36
NG_013031.1:g.9766C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334889.4:c.*376C>T MANE Select ENSP00000334813.3:n.*376C>T
ENST00000256852.7:c.*848C>T ENSP00000256852.7:n.*848C>T
ENST00000334889.3:c.*376C>T ENSP00000334813.3:n.*376C>T
NM_013435.2:c.*376C>T NP_038463.2:n.*376C>T
NM_013435.3:c.*376C>T MANE Select NP_038463.2:n.*376C>T
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