Canonical Allele Identifier: CA2200446074
Gene: SELENOS HGNC NCBI

Linked Data

dbSNP Id: rs2039288805
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.101273179T>G , CM000677.2:g.101273179T>G GRCh38
NC_000015.9:g.101813384T>G , CM000677.1:g.101813384T>G GRCh37
NC_000015.8:g.99630907T>G NCBI36
NG_013322.1:g.9317A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000526049.6:c.485-323A>C MANE Select ENSP00000433541.1:n.485-323A>C
ENST00000398226.7:c.485-323A>C ENSP00000381282.3:n.485-323A>C
ENST00000526043.1:n.1778-323A>C
ENST00000526049.5:c.485-323A>C ENSP00000433541.1:n.485-323A>C
ENST00000528346.1:c.605-323A>C ENSP00000434842.1:n.605-323A>C
ENST00000531964.5:c.416-323A>C ENSP00000433803.1:n.416-323A>C
NM_018445.5:c.485-323A>C NP_060915.2:n.485-323A>C
NM_203472.2:c.485-323A>C NP_982298.2:n.485-323A>C
NM_018445.6:c.485-323A>C MANE Select NP_060915.2:n.485-323A>C
NM_203472.3:c.485-323A>C NP_982298.2:n.485-323A>C
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