Canonical Allele Identifier: CA84786862
Gene: PCOLCE2 HGNC NCBI

Linked Data

dbSNP Id: rs978705085
MyVariant Identifiers: chr3:g.142535198C>T (hg19) chr3:g.142816356C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142816356C>T , CM000665.2:g.142816356C>T GRCh38
NC_000003.11:g.142535198C>T , CM000665.1:g.142535198C>T GRCh37
NC_000003.10:g.144017888C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000470310.5:c.648+179G>A ENSP00000419643.1:n.648+179G>A
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