Canonical Allele Identifier: CA1312515753
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838195T= , CM000664.2:g.182838195T= GRCh38
NC_000002.11:g.183702923T= , CM000664.1:g.183702923T= GRCh37
NC_000002.10:g.183411168T= NCBI36
NG_017197.1:g.33576A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.798-184A= MANE Select ENSP00000295113.4:n.798-184A=
ENST00000295113.4:c.798-184A= ENSP00000295113.4:n.798-184A=
NM_001463.3:c.798-184A= NP_001454.2:n.798-184A=
NM_001463.4:c.798-184A= MANE Select NP_001454.2:n.798-184A=