Canonical Allele Identifier: CA3491072
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs576620135

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339644C>T , CM000667.2:g.146339644C>T GRCh38
NC_000005.9:g.145719207C>T , CM000667.1:g.145719207C>T GRCh37
NC_000005.8:g.145699400C>T NCBI36
NG_011885.1:g.5621C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.217C>T MANE Select ENSP00000495718.1:p.Pro73Ser
ENST00000230732.4:c.217C>T ENSP00000230732.4:p.Pro73Ser
NM_002700.2:c.217C>T NP_002691.1:p.Pro73Ser
NM_002700.3:c.217C>T MANE Select NP_002691.1:p.Pro73Ser