Canonical Allele Identifier: CA1312515883
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838514G= , CM000664.2:g.182838514G= GRCh38
NC_000002.11:g.183703242G= , CM000664.1:g.183703242G= GRCh37
NC_000002.10:g.183411487G= NCBI36
NG_017197.1:g.33257C=

Transcript Alleles

HGVS Amino-acid change
ENST00000295113.5:c.692C= MANE Select ENSP00000295113.4:p.Pro231=
ENST00000295113.4:c.692C= ENSP00000295113.4:p.Pro231=
NM_001463.3:c.692C= NP_001454.2:p.Pro231=
NM_001463.4:c.692C= MANE Select NP_001454.2:p.Pro231=