Canonical Allele Identifier: CA1312515785
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838273A= , CM000664.2:g.182838273A= GRCh38
NC_000002.11:g.183703001A= , CM000664.1:g.183703001A= GRCh37
NC_000002.10:g.183411246A= NCBI36
NG_017197.1:g.33498T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.797+136T= MANE Select ENSP00000295113.4:n.797+136T=
ENST00000295113.4:c.797+136T= ENSP00000295113.4:n.797+136T=
NM_001463.3:c.797+136T= NP_001454.2:n.797+136T=
NM_001463.4:c.797+136T= MANE Select NP_001454.2:n.797+136T=