Canonical Allele Identifier: CA696511
Gene: SELENON HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.25805203G>A
GRCh37 chr1:g.26131694G>A
gnomAD v2:
1:26131694 G / A
gnomAD v3:
1:25805203 G / A
gnomAD v4:
chr1-25805203-G-A
Joint Max Group AF 0.00032319 (MID)
Genomes Max Group AF 0.00007894 (AFR)
Exomes Max Group AF 0.00034129 (MID)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25805203G>A , CM000663.2:g.25805203G>A GRCh38
NC_000001.10:g.26131694G>A , CM000663.1:g.26131694G>A GRCh37
NC_000001.9:g.26004281G>A NCBI36
NG_009930.1:g.10028G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354177.9:c.363G>A ENSP00000346109.5:p.Thr121=
ENST00000494537.2:c.363G>A ENSP00000508308.1:p.Thr121=
ENST00000361547.7:c.465G>A MANE Select ENSP00000355141.2:p.Thr155=
ENST00000354177.8:c.363G>A ENSP00000346109.4:p.Thr121=
ENST00000361547.6:c.465G>A ENSP00000355141.2:p.Thr155=
ENST00000374315.1:c.363G>A ENSP00000363434.1:p.Thr121=
NM_020451.2:c.465G>A NP_065184.2:p.Thr155=
NM_206926.1:c.363G>A NP_996809.1:p.Thr121=
NM_020451.3:c.465G>A MANE Select NP_065184.2:p.Thr155=
NM_206926.2:c.363G>A NP_996809.1:p.Thr121=
Search 100 bp 5'
Search 100 bp 3'