Canonical Allele Identifier: CA361622087
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs1367938001
gnomAD v2: 5-145719723-A-C
gnomAD v4: 5-146340160-A-C
MyVariant Identifiers: chr5:g.145719723A>C (hg19) chr5:g.146340160A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340160A>C , CM000667.2:g.146340160A>C GRCh38
NC_000005.9:g.145719723A>C , CM000667.1:g.145719723A>C GRCh37
NC_000005.8:g.145699916A>C NCBI36
NG_011885.1:g.6137A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.733A>C MANE Select ENSP00000495718.1:p.Lys245Gln
ENST00000230732.4:c.733A>C ENSP00000230732.4:p.Lys245Gln
NM_002700.2:c.733A>C NP_002691.1:p.Lys245Gln
NM_002700.3:c.733A>C MANE Select NP_002691.1:p.Lys245Gln
Search 100 bp 5'
Search 100 bp 3'