Canonical Allele Identifier: CA3491156
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs760441015

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339947C>T , CM000667.2:g.146339947C>T GRCh38
NC_000005.9:g.145719510C>T , CM000667.1:g.145719510C>T GRCh37
NC_000005.8:g.145699703C>T NCBI36
NG_011885.1:g.5924C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.520C>T MANE Select ENSP00000495718.1:p.Pro174Ser
ENST00000230732.4:c.520C>T ENSP00000230732.4:p.Pro174Ser
NM_002700.2:c.520C>T NP_002691.1:p.Pro174Ser
NM_002700.3:c.520C>T MANE Select NP_002691.1:p.Pro174Ser