Canonical Allele Identifier: CA823852349

Gene: POU5F1 PSORS1C3

Linked Data

• dbSNP Id: rs1434099883
• gnomAD v3: 6-31175858-A-G
• gnomAD v4: 6-31175858-A-G
• MyVariant Identifiers: chr6:g.31143635A>G (hg19) ; chr6:g.31175858A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31175858A>G , CM000668.2:g.31175858A>G	GRCh38
NC_000006.11:g.31143635A>G , CM000668.1:g.31143635A>G	GRCh37
NC_000006.10:g.31251614A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000441888.7:c.-184+4761T>C (POU5F1)	ENSP00000389359.2:n.-184+4761T>C
NR_026816.1:n.262-1588T>C (PSORS1C3)
NR_026816.2:n.554-1588T>C (PSORS1C3)
NR_152828.1:n.554-1032T>C (PSORS1C3)
NR_152829.1:n.651T>C (PSORS1C3)
NR_152830.1:n.554-1302T>C (PSORS1C3)
NR_152831.1:n.293-1588T>C (PSORS1C3)
NR_152832.1:n.414-1588T>C (PSORS1C3)
NR_152833.1:n.554-1032T>C (PSORS1C3)
NR_152834.1:n.651T>C (PSORS1C3)
NR_152835.1:n.293-1825T>C (PSORS1C3)
NR_152836.1:n.554-1302T>C (PSORS1C3)
NR_152837.1:n.554-1179T>C (PSORS1C3)
NR_152838.1:n.651T>C (PSORS1C3)
NR_152839.1:n.553+1781T>C (PSORS1C3)