Canonical Allele Identifier: CA1312515996
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838776T= , CM000664.2:g.182838776T= GRCh38
NC_000002.11:g.183703504T= , CM000664.1:g.183703504T= GRCh37
NC_000002.10:g.183411749T= NCBI36
NG_017197.1:g.32995A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-163A= MANE Select ENSP00000295113.4:n.593-163A=
ENST00000295113.4:c.593-163A= ENSP00000295113.4:n.593-163A=
NM_001463.3:c.593-163A= NP_001454.2:n.593-163A=
NM_001463.4:c.593-163A= MANE Select NP_001454.2:n.593-163A=