Canonical Allele Identifier: CA17286847
Gene: PARK7 HGNC NCBI

Linked Data

dbSNP Id: rs769196724
gnomAD v4: 1-7985320-A-T
MyVariant Identifiers: chr1:g.8045380A>T (hg19) chr1:g.7985320A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7985320A>T , CM000663.2:g.7985320A>T GRCh38
NC_000001.10:g.8045380A>T , CM000663.1:g.8045380A>T GRCh37
NC_000001.9:g.7967967A>T NCBI36
NG_008271.1:g.28667A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.*266A>T MANE Select ENSP00000340278.5:n.*266A>T
ENST00000493678.5:c.*266A>T ENSP00000418770.1:n.*266A>T
NM_007262.5:c.*266A>T MANE Select NP_009193.2:n.*266A>T
NM_001123377.2:c.*266A>T NP_001116849.1:n.*266A>T
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