Canonical Allele Identifier: CA361621762
Gene: POU4F3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.145719654T>G (hg19) chr5:g.146340091T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340091T>G , CM000667.2:g.146340091T>G GRCh38
NC_000005.9:g.145719654T>G , CM000667.1:g.145719654T>G GRCh37
NC_000005.8:g.145699847T>G NCBI36
NG_011885.1:g.6068T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.664T>G MANE Select ENSP00000495718.1:p.Ser222Ala
ENST00000230732.4:c.664T>G ENSP00000230732.4:p.Ser222Ala
NM_002700.2:c.664T>G NP_002691.1:p.Ser222Ala
NM_002700.3:c.664T>G MANE Select NP_002691.1:p.Ser222Ala
Search 100 bp 5'
Search 100 bp 3'