Canonical Allele Identifier: CA1312515977
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838727C= , CM000664.2:g.182838727C= GRCh38
NC_000002.11:g.183703455C= , CM000664.1:g.183703455C= GRCh37
NC_000002.10:g.183411700C= NCBI36
NG_017197.1:g.33044G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-114G= MANE Select ENSP00000295113.4:n.593-114G=
ENST00000295113.4:c.593-114G= ENSP00000295113.4:n.593-114G=
NM_001463.3:c.593-114G= NP_001454.2:n.593-114G=
NM_001463.4:c.593-114G= MANE Select NP_001454.2:n.593-114G=