Canonical Allele Identifier: CA1312516024
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838838G= , CM000664.2:g.182838838G= GRCh38
NC_000002.11:g.183703566G= , CM000664.1:g.183703566G= GRCh37
NC_000002.10:g.183411811G= NCBI36
NG_017197.1:g.32933C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-225C= MANE Select ENSP00000295113.4:n.593-225C=
ENST00000295113.4:c.593-225C= ENSP00000295113.4:n.593-225C=
NM_001463.3:c.593-225C= NP_001454.2:n.593-225C=
NM_001463.4:c.593-225C= MANE Select NP_001454.2:n.593-225C=