Canonical Allele Identifier: CA823852252

Gene: POU5F1 PSORS1C3

Linked Data

• dbSNP Id: rs1269134963
• gnomAD v3: 6-31175597-T-C
• gnomAD v4: 6-31175597-T-C
• MyVariant Identifiers: chr6:g.31143374T>C (hg19) ; chr6:g.31175597T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31175597T>C , CM000668.2:g.31175597T>C	GRCh38
NC_000006.11:g.31143374T>C , CM000668.1:g.31143374T>C	GRCh37
NC_000006.10:g.31251353T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441888.7:c.-184+5022A>G (POU5F1)	ENSP00000389359.2:n.-184+5022A>G
NR_026816.1:n.262-1327A>G (PSORS1C3)
NR_026816.2:n.554-1327A>G (PSORS1C3)
NR_152828.1:n.554-771A>G (PSORS1C3)
NR_152829.1:n.820+92A>G (PSORS1C3)
NR_152830.1:n.554-1041A>G (PSORS1C3)
NR_152831.1:n.293-1327A>G (PSORS1C3)
NR_152832.1:n.414-1327A>G (PSORS1C3)
NR_152833.1:n.554-771A>G (PSORS1C3)
NR_152834.1:n.820+92A>G (PSORS1C3)
NR_152835.1:n.293-1564A>G (PSORS1C3)
NR_152836.1:n.554-1041A>G (PSORS1C3)
NR_152837.1:n.554-918A>G (PSORS1C3)
NR_152838.1:n.820+92A>G (PSORS1C3)
NR_152839.1:n.554-1564A>G (PSORS1C3)