Canonical Allele Identifier: CA2200446334
Gene: SELENOS HGNC NCBI

Linked Data

dbSNP Id: rs2039294362
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.101273728A>G , CM000677.2:g.101273728A>G GRCh38
NC_000015.9:g.101813933A>G , CM000677.1:g.101813933A>G GRCh37
NC_000015.8:g.99631456A>G NCBI36
NG_013322.1:g.8768T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000526049.6:c.484+692T>C MANE Select ENSP00000433541.1:n.484+692T>C
ENST00000398226.7:c.484+692T>C ENSP00000381282.3:n.484+692T>C
ENST00000526043.1:n.1777+692T>C
ENST00000526049.5:c.484+692T>C ENSP00000433541.1:n.484+692T>C
ENST00000528346.1:c.604+692T>C ENSP00000434842.1:n.604+692T>C
ENST00000531964.5:c.415+692T>C ENSP00000433803.1:n.415+692T>C
NM_018445.5:c.484+692T>C NP_060915.2:n.484+692T>C
NM_203472.2:c.484+692T>C NP_982298.2:n.484+692T>C
NM_018445.6:c.484+692T>C MANE Select NP_060915.2:n.484+692T>C
NM_203472.3:c.484+692T>C NP_982298.2:n.484+692T>C
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