Canonical Allele Identifier: CA850466707
Gene: PNOC HGNC NCBI

Linked Data

dbSNP Id: rs1406324722
MyVariant Identifiers: chr8:g.28181783G>A (hg19) chr8:g.28324266G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.28324266G>A , CM000670.2:g.28324266G>A GRCh38
NC_000008.10:g.28181783G>A , CM000670.1:g.28181783G>A GRCh37
NC_000008.9:g.28237702G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000301908.8:c.-23-4869G>A MANE Select ENSP00000301908.3:n.-23-4869G>A
ENST00000301908.7:c.-23-4869G>A ENSP00000301908.3:n.-23-4869G>A
ENST00000518479.5:c.-23-4869G>A ENSP00000428059.1:n.-23-4869G>A
NM_006228.4:c.-23-4869G>A NP_006219.1:n.-23-4869G>A
XM_005273532.1:c.-23-4869G>A XP_005273589.1:n.-23-4869G>A
XM_011544559.1:c.-23-4869G>A XP_011542861.1:n.-23-4869G>A
XM_005273532.2:c.-23-4869G>A XP_005273589.1:n.-23-4869G>A
XM_011544559.2:c.-23-4869G>A XP_011542861.1:n.-23-4869G>A
NM_006228.5:c.-23-4869G>A MANE Select NP_006219.1:n.-23-4869G>A
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