Canonical Allele Identifier: CA119478162
Gene: PART1 HGNC NCBI

Linked Data

dbSNP Id: rs190512680
gnomAD v3: 5-60529420-T-C
gnomAD v4: 5-60529420-T-C
MyVariant Identifiers: chr5:g.59825247T>C (hg19) chr5:g.60529420T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529420T>C , CM000667.2:g.60529420T>C GRCh38
NC_000005.9:g.59825247T>C , CM000667.1:g.59825247T>C GRCh37
NC_000005.8:g.59861004T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.728T>C
Search 100 bp 5'
Search 100 bp 3'