Canonical Allele Identifier: CA361621997

Gene: POU4F3

Linked Data

• gnomAD v4: 5-146340136-T-C
• MyVariant Identifiers: chr5:g.145719699T>C (hg19) ; chr5:g.146340136T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.146340136T>C , CM000667.2:g.146340136T>C	GRCh38
NC_000005.9:g.145719699T>C , CM000667.1:g.145719699T>C	GRCh37
NC_000005.8:g.145699892T>C	NCBI36
NG_011885.1:g.6113T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646991.2:c.709T>C MANE Select	ENSP00000495718.1:p.Ser237Pro
ENST00000230732.4:c.709T>C	ENSP00000230732.4:p.Ser237Pro
NM_002700.2:c.709T>C	NP_002691.1:p.Ser237Pro
NM_002700.3:c.709T>C MANE Select	NP_002691.1:p.Ser237Pro