Canonical Allele Identifier: CA504297019
Gene: RAX HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56936371G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59269139G>C , CM000680.2:g.59269139G>C GRCh38
NC_000018.9:g.56936371G>C , CM000680.1:g.56936371G>C GRCh37
NC_000018.8:g.55087351G>C NCBI36
NG_013031.1:g.9255C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000334889.4:c.906C>G MANE Select ENSP00000334813.3:p.Ser302=
ENST00000256852.7:c.*337C>G ENSP00000256852.7:n.*337C>G
ENST00000334889.3:c.906C>G ENSP00000334813.3:p.Ser302=
NM_013435.2:c.906C>G NP_038463.2:p.Ser302=
NM_013435.3:c.906C>G MANE Select NP_038463.2:p.Ser302=
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Search 100 bp 3'