Canonical Allele Identifier: CA1312515997
Gene: FRZB HGNC NCBI

Linked Data

dbSNP Id: rs1695555839

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838776T>C , CM000664.2:g.182838776T>C GRCh38
NC_000002.11:g.183703504T>C , CM000664.1:g.183703504T>C GRCh37
NC_000002.10:g.183411749T>C NCBI36
NG_017197.1:g.32995A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-163A>G MANE Select ENSP00000295113.4:n.593-163A>G
ENST00000295113.4:c.593-163A>G ENSP00000295113.4:n.593-163A>G
NM_001463.3:c.593-163A>G NP_001454.2:n.593-163A>G
NM_001463.4:c.593-163A>G MANE Select NP_001454.2:n.593-163A>G