Canonical Allele Identifier: CA1381534895
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs1706569736
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264231A>G , CM000665.2:g.87264231A>G GRCh38
NC_000003.11:g.87313381A>G , CM000665.1:g.87313381A>G GRCh37
NC_000003.10:g.87396071A>G NCBI36
NG_008225.2:g.17357T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.517+57T>C ENSP00000342931.3:n.517+57T>C
ENST00000350375.7:c.439+57T>C MANE Select ENSP00000263781.2:n.439+57T>C
ENST00000344265.7:c.517+57T>C ENSP00000342931.3:n.517+57T>C
ENST00000350375.6:c.439+57T>C ENSP00000263781.2:n.439+57T>C
ENST00000560656.1:c.439+57T>C ENSP00000452610.1:n.439+57T>C
ENST00000561167.5:c.215-1996T>C ENSP00000454072.1:n.215-1996T>C
NM_000306.3:c.439+57T>C NP_000297.1:n.439+57T>C
NM_001122757.2:c.517+57T>C NP_001116229.1:n.517+57T>C
NM_000306.4:c.439+57T>C MANE Select NP_000297.1:n.439+57T>C
NM_001122757.3:c.517+57T>C NP_001116229.1:n.517+57T>C
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