Canonical Allele Identifier: CA151078370
Gene: SOD2 HGNC NCBI

Linked Data

dbSNP Id: rs150578308
gnomAD v2: 6-160098106-T-C
gnomAD v3: 6-159677074-T-C
gnomAD v4: 6-159677074-T-C
MyVariant Identifiers: chr6:g.160098106T>C (hg19) chr6:g.159677074T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.159677074T>C , CM000668.2:g.159677074T>C GRCh38
NC_000006.11:g.160098106T>C , CM000668.1:g.160098106T>C GRCh37
NC_000006.10:g.160018096T>C NCBI36
NG_008729.3:g.90456A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000538183.7:c.*5419A>G MANE Select ENSP00000446252.1:n.*5419A>G
ENST00000538183.6:c.*5419A>G ENSP00000446252.1:n.*5419A>G
NM_000636.4:c.*5419A>G MANE Select NP_000627.2:n.*5419A>G
NM_001322814.2:c.*5419A>G NP_001309743.1:n.*5419A>G
NM_001322815.2:c.*5419A>G NP_001309744.1:n.*5419A>G
NM_001322819.2:c.*5419A>G NP_001309748.1:n.*5419A>G
NM_001322820.2:c.*5419A>G NP_001309749.1:n.*5419A>G
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