Canonical Allele Identifier: CA1312515973
Gene: FRZB HGNC NCBI

Linked Data

dbSNP Id: rs1695555350
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838714A>T , CM000664.2:g.182838714A>T GRCh38
NC_000002.11:g.183703442A>T , CM000664.1:g.183703442A>T GRCh37
NC_000002.10:g.183411687A>T NCBI36
NG_017197.1:g.33057T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-101T>A MANE Select ENSP00000295113.4:n.593-101T>A
ENST00000295113.4:c.593-101T>A ENSP00000295113.4:n.593-101T>A
NM_001463.3:c.593-101T>A NP_001454.2:n.593-101T>A
NM_001463.4:c.593-101T>A MANE Select NP_001454.2:n.593-101T>A
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