Canonical Allele Identifier: CA2200446279
Gene: SELENOS HGNC NCBI

Linked Data

dbSNP Id: rs2039293372
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.101273621C>G , CM000677.2:g.101273621C>G GRCh38
NC_000015.9:g.101813826C>G , CM000677.1:g.101813826C>G GRCh37
NC_000015.8:g.99631349C>G NCBI36
NG_013322.1:g.8875G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000526049.6:c.485-765G>C MANE Select ENSP00000433541.1:n.485-765G>C
ENST00000398226.7:c.485-765G>C ENSP00000381282.3:n.485-765G>C
ENST00000526043.1:n.1778-765G>C
ENST00000526049.5:c.485-765G>C ENSP00000433541.1:n.485-765G>C
ENST00000528346.1:c.605-765G>C ENSP00000434842.1:n.605-765G>C
ENST00000531964.5:c.416-765G>C ENSP00000433803.1:n.416-765G>C
NM_018445.5:c.485-765G>C NP_060915.2:n.485-765G>C
NM_203472.2:c.485-765G>C NP_982298.2:n.485-765G>C
NM_018445.6:c.485-765G>C MANE Select NP_060915.2:n.485-765G>C
NM_203472.3:c.485-765G>C NP_982298.2:n.485-765G>C
Search 100 bp 5'
Search 100 bp 3'