Canonical Allele Identifier: CA444546139
Gene: PART1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.59825243T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529416T>G , CM000667.2:g.60529416T>G GRCh38
NC_000005.9:g.59825243T>G , CM000667.1:g.59825243T>G GRCh37
NC_000005.8:g.59861000T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024617.1:n.724T>G
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