Canonical Allele Identifier: CA1312515882
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838513T= , CM000664.2:g.182838513T= GRCh38
NC_000002.11:g.183703241T= , CM000664.1:g.183703241T= GRCh37
NC_000002.10:g.183411486T= NCBI36
NG_017197.1:g.33258A=

Transcript Alleles

HGVS Amino-acid change
ENST00000295113.5:c.693A= MANE Select ENSP00000295113.4:p.Pro231=
ENST00000295113.4:c.693A= ENSP00000295113.4:p.Pro231=
NM_001463.3:c.693A= NP_001454.2:p.Pro231=
NM_001463.4:c.693A= MANE Select NP_001454.2:p.Pro231=