Canonical Allele Identifier: CA1773202750
Gene: PNOC HGNC NCBI

Linked Data

dbSNP Id: rs1801190572
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.28324300A>G , CM000670.2:g.28324300A>G GRCh38
NC_000008.10:g.28181817A>G , CM000670.1:g.28181817A>G GRCh37
NC_000008.9:g.28237736A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000301908.8:c.-23-4835A>G MANE Select ENSP00000301908.3:n.-23-4835A>G
ENST00000301908.7:c.-23-4835A>G ENSP00000301908.3:n.-23-4835A>G
ENST00000518479.5:c.-23-4835A>G ENSP00000428059.1:n.-23-4835A>G
NM_006228.4:c.-23-4835A>G NP_006219.1:n.-23-4835A>G
XM_005273532.1:c.-23-4835A>G XP_005273589.1:n.-23-4835A>G
XM_011544559.1:c.-23-4835A>G XP_011542861.1:n.-23-4835A>G
XM_005273532.2:c.-23-4835A>G XP_005273589.1:n.-23-4835A>G
XM_011544559.2:c.-23-4835A>G XP_011542861.1:n.-23-4835A>G
NM_006228.5:c.-23-4835A>G MANE Select NP_006219.1:n.-23-4835A>G
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