Canonical Allele Identifier: CA1312515969
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838707C= , CM000664.2:g.182838707C= GRCh38
NC_000002.11:g.183703435C= , CM000664.1:g.183703435C= GRCh37
NC_000002.10:g.183411680C= NCBI36
NG_017197.1:g.33064G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-94G= MANE Select ENSP00000295113.4:n.593-94G=
ENST00000295113.4:c.593-94G= ENSP00000295113.4:n.593-94G=
NM_001463.3:c.593-94G= NP_001454.2:n.593-94G=
NM_001463.4:c.593-94G= MANE Select NP_001454.2:n.593-94G=