Canonical Allele Identifier: CA697096606
Gene: POMP HGNC NCBI

Linked Data

dbSNP Id: rs1469029441
gnomAD v3: 13-28659019-G-A
gnomAD v4: 13-28659019-G-A
MyVariant Identifiers: chr13:g.29233156G>A (hg19) chr13:g.28659019G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28659019G>A , CM000675.2:g.28659019G>A GRCh38
NC_000013.10:g.29233156G>A , CM000675.1:g.29233156G>A GRCh37
NC_000013.9:g.28131156G>A NCBI36
NG_027550.1:g.5016G>A

Transcript Alleles

HGVS Amino-acid Change
NM_015932.5:c.-166G>A NP_057016.1:n.-166G>A
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