Canonical Allele Identifier: CA1312515961
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838694_182838695delinsTC , CM000664.2:g.182838694_182838695delinsTC GRCh38
NC_000002.11:g.183703422_183703423delinsTC , CM000664.1:g.183703422_183703423delinsTC GRCh37
NC_000002.10:g.183411667_183411668delinsTC NCBI36
NG_017197.1:g.33076_33077delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-82_593-81delinsGA MANE Select ENSP00000295113.4:n.593-82_593-81delinsGA
ENST00000295113.4:c.593-82_593-81delinsGA ENSP00000295113.4:n.593-82_593-81delinsGA
NM_001463.3:c.593-82_593-81delinsGA NP_001454.2:n.593-82_593-81delinsGA
NM_001463.4:c.593-82_593-81delinsGA MANE Select NP_001454.2:n.593-82_593-81delinsGA