Canonical Allele Identifier: CA3491140
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs755969670
ExAC: 5:145719465 A / G
gnomAD v2: 5-145719465-A-G
gnomAD v4: 5-146339902-A-G
MyVariant Identifiers: chr5:g.145719465A>G (hg19) chr5:g.146339902A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339902A>G , CM000667.2:g.146339902A>G GRCh38
NC_000005.9:g.145719465A>G , CM000667.1:g.145719465A>G GRCh37
NC_000005.8:g.145699658A>G NCBI36
NG_011885.1:g.5879A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.475A>G MANE Select ENSP00000495718.1:p.Met159Val
ENST00000230732.4:c.475A>G ENSP00000230732.4:p.Met159Val
NM_002700.2:c.475A>G NP_002691.1:p.Met159Val
NM_002700.3:c.475A>G MANE Select NP_002691.1:p.Met159Val
Search 100 bp 5'
Search 100 bp 3'