Canonical Allele Identifier: CA10647975

Gene: RAX

Linked Data

• ClinVar Variation Id: 327523
• ClinVar RCV Id: RCV000350939
• dbSNP Id: rs45501496
• gnomAD v2: 18-56935328-A-G
• gnomAD v3: 18-59268096-A-G
• gnomAD v4: 18-59268096-A-G
• MyVariant Identifiers: chr18:g.56935328A>G (hg19) ; chr18:g.59268096A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59268096A>G , CM000680.2:g.59268096A>G	GRCh38
NC_000018.9:g.56935328A>G , CM000680.1:g.56935328A>G	GRCh37
NC_000018.8:g.55086308A>G	NCBI36
NG_013031.1:g.10298T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334889.4:c.*908T>C MANE Select	ENSP00000334813.3:n.*908T>C
ENST00000256852.7:c.*1380T>C	ENSP00000256852.7:n.*1380T>C
ENST00000334889.3:c.*908T>C	ENSP00000334813.3:n.*908T>C
NM_013435.2:c.*908T>C	NP_038463.2:n.*908T>C
NM_013435.3:c.*908T>C MANE Select	NP_038463.2:n.*908T>C