Canonical Allele Identifier: CA504297031
Gene: RAX HGNC NCBI

Linked Data

gnomAD v4: 18-59269142-G-T
MyVariant Identifiers: chr18:g.56936374G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59269142G>T , CM000680.2:g.59269142G>T GRCh38
NC_000018.9:g.56936374G>T , CM000680.1:g.56936374G>T GRCh37
NC_000018.8:g.55087354G>T NCBI36
NG_013031.1:g.9252C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000334889.4:c.903C>A MANE Select ENSP00000334813.3:p.Pro301=
ENST00000256852.7:c.*334C>A ENSP00000256852.7:n.*334C>A
ENST00000334889.3:c.903C>A ENSP00000334813.3:p.Pro301=
NM_013435.2:c.903C>A NP_038463.2:p.Pro301=
NM_013435.3:c.903C>A MANE Select NP_038463.2:p.Pro301=
Search 100 bp 5'
Search 100 bp 3'