Canonical Allele Identifier: CA1312515832
Gene: FRZB HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838409C= , CM000664.2:g.182838409C= GRCh38
NC_000002.11:g.183703137C= , CM000664.1:g.183703137C= GRCh37
NC_000002.10:g.183411382C= NCBI36
NG_017197.1:g.33362G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.797G= MANE Select ENSP00000295113.4:p.Arg266=
ENST00000295113.4:c.797G= ENSP00000295113.4:p.Arg266=
NM_001463.3:c.797G= NP_001454.2:p.Arg266=
NM_001463.4:c.797G= MANE Select NP_001454.2:p.Arg266=
Search 100 bp 5'
Search 100 bp 3'