Canonical Allele Identifier: CA356638863
Gene: SOD3 HGNC NCBI

Linked Data

gnomAD v4: 4-24799762-G-T
MyVariant Identifiers: chr4:g.24801384G>T (hg19) chr4:g.24799762G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.24799762G>T , CM000666.2:g.24799762G>T GRCh38
NC_000004.11:g.24801384G>T , CM000666.1:g.24801384G>T GRCh37
NC_000004.10:g.24410482G>T NCBI36
NG_012213.1:g.9300G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382120.4:c.241G>T MANE Select ENSP00000371554.3:p.Val81Phe
ENST00000382120.3:c.241G>T ENSP00000371554.3:p.Val81Phe
NM_003102.2:c.241G>T NP_003093.2:p.Val81Phe
XR_427488.1:n.431G>T
NM_003102.3:c.241G>T NP_003093.2:p.Val81Phe
NM_003102.4:c.241G>T MANE Select NP_003093.2:p.Val81Phe
Search 100 bp 5'
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