Canonical Allele Identifier: CA247677203
Gene: POMP HGNC NCBI

Linked Data

dbSNP Id: rs975171789
MyVariant Identifiers: chr13:g.29233158C>G (hg19) chr13:g.28659021C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28659021C>G , CM000675.2:g.28659021C>G GRCh38
NC_000013.10:g.29233158C>G , CM000675.1:g.29233158C>G GRCh37
NC_000013.9:g.28131158C>G NCBI36
NG_027550.1:g.5018C>G

Transcript Alleles

HGVS Amino-acid change
NM_015932.5:c.-164C>G NP_057016.1:n.-164C>G
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