Canonical Allele Identifier: CA2701210320
Gene: FRZB HGNC NCBI

Linked Data

dbSNP Id: rs2105752240

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838783T>C , CM000664.2:g.182838783T>C GRCh38
NC_000002.11:g.183703511T>C , CM000664.1:g.183703511T>C GRCh37
NC_000002.10:g.183411756T>C NCBI36
NG_017197.1:g.32988A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-170A>G MANE Select ENSP00000295113.4:n.593-170A>G
ENST00000295113.4:c.593-170A>G ENSP00000295113.4:n.593-170A>G
NM_001463.3:c.593-170A>G NP_001454.2:n.593-170A>G
NM_001463.4:c.593-170A>G MANE Select NP_001454.2:n.593-170A>G