Canonical Allele Identifier: CA1312515915
Gene: FRZB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838585C= , CM000664.2:g.182838585C= GRCh38
NC_000002.11:g.183703313C= , CM000664.1:g.183703313C= GRCh37
NC_000002.10:g.183411558C= NCBI36
NG_017197.1:g.33186G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.621G= MANE Select ENSP00000295113.4:p.Lys207=
ENST00000295113.4:c.621G= ENSP00000295113.4:p.Lys207=
NM_001463.3:c.621G= NP_001454.2:p.Lys207=
NM_001463.4:c.621G= MANE Select NP_001454.2:p.Lys207=
Search 100 bp 5'
Search 100 bp 3'