Canonical Allele Identifier: CA1312515889
Gene: FRZB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838530A= , CM000664.2:g.182838530A= GRCh38
NC_000002.11:g.183703258A= , CM000664.1:g.183703258A= GRCh37
NC_000002.10:g.183411503A= NCBI36
NG_017197.1:g.33241T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.676T= MANE Select ENSP00000295113.4:p.Ser226=
ENST00000295113.4:c.676T= ENSP00000295113.4:p.Ser226=
NM_001463.3:c.676T= NP_001454.2:p.Ser226=
NM_001463.4:c.676T= MANE Select NP_001454.2:p.Ser226=
Search 100 bp 5'
Search 100 bp 3'