Canonical Allele Identifier: CA2731698675
Gene: SELENOS HGNC NCBI

Linked Data

dbSNP Id: rs2141296640
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.101273665C>T , CM000677.2:g.101273665C>T GRCh38
NC_000015.9:g.101813870C>T , CM000677.1:g.101813870C>T GRCh37
NC_000015.8:g.99631393C>T NCBI36
NG_013322.1:g.8831G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000526049.6:c.484+755G>A MANE Select ENSP00000433541.1:n.484+755G>A
ENST00000398226.7:c.484+755G>A ENSP00000381282.3:n.484+755G>A
ENST00000526043.1:n.1777+755G>A
ENST00000526049.5:c.484+755G>A ENSP00000433541.1:n.484+755G>A
ENST00000528346.1:c.604+755G>A ENSP00000434842.1:n.604+755G>A
ENST00000531964.5:c.415+755G>A ENSP00000433803.1:n.415+755G>A
NM_018445.5:c.484+755G>A NP_060915.2:n.484+755G>A
NM_203472.2:c.484+755G>A NP_982298.2:n.484+755G>A
NM_018445.6:c.484+755G>A MANE Select NP_060915.2:n.484+755G>A
NM_203472.3:c.484+755G>A NP_982298.2:n.484+755G>A
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