Canonical Allele Identifier: CA119478144
Gene: PART1 HGNC NCBI

Linked Data

dbSNP Id: rs1013068827
MyVariant Identifiers: chr5:g.59825074T>C (hg19) chr5:g.60529247T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529247T>C , CM000667.2:g.60529247T>C GRCh38
NC_000005.9:g.59825074T>C , CM000667.1:g.59825074T>C GRCh37
NC_000005.8:g.59860831T>C NCBI36
NG_027957.2:g.83A>G

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.712-157T>C
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