Canonical Allele Identifier: CA850466710

Gene: PNOC

Linked Data

• dbSNP Id: rs1162604708
• gnomAD v3: 8-28324275-A-T
• gnomAD v4: 8-28324275-A-T
• MyVariant Identifiers: chr8:g.28181792A>T (hg19) ; chr8:g.28324275A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28324275A>T , CM000670.2:g.28324275A>T	GRCh38
NC_000008.10:g.28181792A>T , CM000670.1:g.28181792A>T	GRCh37
NC_000008.9:g.28237711A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000301908.8:c.-23-4860A>T MANE Select	ENSP00000301908.3:n.-23-4860A>T
ENST00000301908.7:c.-23-4860A>T	ENSP00000301908.3:n.-23-4860A>T
ENST00000518479.5:c.-23-4860A>T	ENSP00000428059.1:n.-23-4860A>T
NM_006228.4:c.-23-4860A>T	NP_006219.1:n.-23-4860A>T
XM_005273532.1:c.-23-4860A>T	XP_005273589.1:n.-23-4860A>T
XM_011544559.1:c.-23-4860A>T	XP_011542861.1:n.-23-4860A>T
XM_005273532.2:c.-23-4860A>T	XP_005273589.1:n.-23-4860A>T
XM_011544559.2:c.-23-4860A>T	XP_011542861.1:n.-23-4860A>T
NM_006228.5:c.-23-4860A>T MANE Select	NP_006219.1:n.-23-4860A>T