Canonical Allele Identifier: CA10606958
Gene: SELENON HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.25800237C>A
GRCh37 chr1:g.26126728C>A
gnomAD v2:
1:26126728 C / A
gnomAD v3:
1:25800237 C / A
gnomAD v4:
chr1-25800237-C-A
Joint Max Group AF 0.00049891 (AFR)
Genomes Max Group AF 0.00044651 (AFR)
Exomes Max Group AF 0.00042668 (AFR)
ClinVar RCV:
RCV000259857
RCV001086966
ClinVar Variation:
290956
dbSNP:
866566089
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25800237C>A , CM000663.2:g.25800237C>A GRCh38
NC_000001.10:g.26126728C>A , CM000663.1:g.26126728C>A GRCh37
NC_000001.9:g.25999315C>A NCBI36
NG_009930.1:g.5062C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354177.9:c.7C>A ENSP00000346109.5:p.Arg3=
ENST00000494537.2:c.7C>A ENSP00000508308.1:p.Arg3=
ENST00000361547.7:c.7C>A MANE Select ENSP00000355141.2:p.Arg3=
ENST00000354177.8:c.7C>A ENSP00000346109.4:p.Arg3=
ENST00000361547.6:c.7C>A ENSP00000355141.2:p.Arg3=
ENST00000374315.1:c.7C>A ENSP00000363434.1:p.Arg3=
NM_020451.2:c.7C>A NP_065184.2:p.Arg3=
NM_206926.1:c.7C>A NP_996809.1:p.Arg3=
NM_020451.3:c.7C>A MANE Select NP_065184.2:p.Arg3=
NM_206926.2:c.7C>A NP_996809.1:p.Arg3=
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