Canonical Allele Identifier: CA504297012
Gene: RAX HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.56936368G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59269136G>A , CM000680.2:g.59269136G>A GRCh38
NC_000018.9:g.56936368G>A , CM000680.1:g.56936368G>A GRCh37
NC_000018.8:g.55087348G>A NCBI36
NG_013031.1:g.9258C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000334889.4:c.909C>T MANE Select ENSP00000334813.3:p.Tyr303=
ENST00000256852.7:c.*340C>T ENSP00000256852.7:n.*340C>T
ENST00000334889.3:c.909C>T ENSP00000334813.3:p.Tyr303=
NM_013435.2:c.909C>T NP_038463.2:p.Tyr303=
NM_013435.3:c.909C>T MANE Select NP_038463.2:p.Tyr303=
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