Canonical Allele Identifier: CA1312515821
Gene: FRZB HGNC NCBI

Linked Data

dbSNP Id: rs1695550167
gnomAD v4: 2-182838381-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838381T>C , CM000664.2:g.182838381T>C GRCh38
NC_000002.11:g.183703109T>C , CM000664.1:g.183703109T>C GRCh37
NC_000002.10:g.183411354T>C NCBI36
NG_017197.1:g.33390A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.797+28A>G MANE Select ENSP00000295113.4:n.797+28A>G
ENST00000295113.4:c.797+28A>G ENSP00000295113.4:n.797+28A>G
NM_001463.3:c.797+28A>G NP_001454.2:n.797+28A>G
NM_001463.4:c.797+28A>G MANE Select NP_001454.2:n.797+28A>G
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