Canonical Allele Identifier: CA19698400
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 2038343
ClinVar RCV Id: RCV002890692
dbSNP Id: rs945683594
gnomAD v2: 1-26135590-C-G
gnomAD v3: 1-25809099-C-G
gnomAD v4: 1-25809099-C-G
MyVariant Identifiers: chr1:g.26135590C>G (hg19) chr1:g.25809099C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809099C>G , CM000663.2:g.25809099C>G GRCh38
NC_000001.10:g.26135590C>G , CM000663.1:g.26135590C>G GRCh37
NC_000001.9:g.26008177C>G NCBI36
NG_009930.1:g.13924C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000354177.9:c.650C>G ENSP00000346109.5:p.Ala217Gly
ENST00000494537.2:c.719C>G ENSP00000508308.1:p.Ala240Gly
ENST00000361547.7:c.821C>G MANE Select ENSP00000355141.2:p.Ala274Gly
ENST00000354177.8:c.719C>G ENSP00000346109.4:p.Ala240Gly
ENST00000361547.6:c.821C>G ENSP00000355141.2:p.Ala274Gly
ENST00000374315.1:c.719C>G ENSP00000363434.1:p.Ala240Gly
NM_020451.2:c.821C>G NP_065184.2:p.Ala274Gly
NM_206926.1:c.719C>G NP_996809.1:p.Ala240Gly
NM_020451.3:c.821C>G MANE Select NP_065184.2:p.Ala274Gly
NM_206926.2:c.719C>G NP_996809.1:p.Ala240Gly
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