Canonical Allele Identifier: CA1312515786
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838280C= , CM000664.2:g.182838280C= GRCh38
NC_000002.11:g.183703008C= , CM000664.1:g.183703008C= GRCh37
NC_000002.10:g.183411253C= NCBI36
NG_017197.1:g.33491G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.797+129G= MANE Select ENSP00000295113.4:n.797+129G=
ENST00000295113.4:c.797+129G= ENSP00000295113.4:n.797+129G=
NM_001463.3:c.797+129G= NP_001454.2:n.797+129G=
NM_001463.4:c.797+129G= MANE Select NP_001454.2:n.797+129G=