Canonical Allele Identifier: CA361620638
Gene: POU4F3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.145719399C>A (hg19) chr5:g.146339836C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339836C>A , CM000667.2:g.146339836C>A GRCh38
NC_000005.9:g.145719399C>A , CM000667.1:g.145719399C>A GRCh37
NC_000005.8:g.145699592C>A NCBI36
NG_011885.1:g.5813C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.409C>A MANE Select ENSP00000495718.1:p.His137Asn
ENST00000230732.4:c.409C>A ENSP00000230732.4:p.His137Asn
NM_002700.2:c.409C>A NP_002691.1:p.His137Asn
NM_002700.3:c.409C>A MANE Select NP_002691.1:p.His137Asn
Search 100 bp 5'
Search 100 bp 3'