Canonical Allele Identifier: CA1549819702
Gene: PART1 HGNC NCBI

Linked Data

dbSNP Id: rs1014103770
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529252C>G , CM000667.2:g.60529252C>G GRCh38
NC_000005.9:g.59825079C>G , CM000667.1:g.59825079C>G GRCh37
NC_000005.8:g.59860836C>G NCBI36
NG_027957.2:g.78G>C

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.712-152C>G
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