Canonical Allele Identifier: CA3491148
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs769197405

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339932C>G , CM000667.2:g.146339932C>G GRCh38
NC_000005.9:g.145719495C>G , CM000667.1:g.145719495C>G GRCh37
NC_000005.8:g.145699688C>G NCBI36
NG_011885.1:g.5909C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.505C>G MANE Select ENSP00000495718.1:p.Pro169Ala
ENST00000230732.4:c.505C>G ENSP00000230732.4:p.Pro169Ala
NM_002700.2:c.505C>G NP_002691.1:p.Pro169Ala
NM_002700.3:c.505C>G MANE Select NP_002691.1:p.Pro169Ala