Canonical Allele Identifier: CA2753437685
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838279dup , CM000664.2:g.182838279dup GRCh38
NC_000002.11:g.183703007dup , CM000664.1:g.183703007dup GRCh37
NC_000002.10:g.183411252dup NCBI36
NG_017197.1:g.33495dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.797+133dup MANE Select ENSP00000295113.4:n.797+133dup
ENST00000295113.4:c.797+133dup ENSP00000295113.4:n.797+133dup
NM_001463.3:c.797+133dup NP_001454.2:n.797+133dup
NM_001463.4:c.797+133dup MANE Select NP_001454.2:n.797+133dup