Canonical Allele Identifier: CA2511278858
Gene: FRZB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838256T>A , CM000664.2:g.182838256T>A GRCh38
NC_000002.11:g.183702984T>A , CM000664.1:g.183702984T>A GRCh37
NC_000002.10:g.183411229T>A NCBI36
NG_017197.1:g.33515A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.797+153A>T MANE Select ENSP00000295113.4:n.797+153A>T
ENST00000295113.4:c.797+153A>T ENSP00000295113.4:n.797+153A>T
NM_001463.3:c.797+153A>T NP_001454.2:n.797+153A>T
NM_001463.4:c.797+153A>T MANE Select NP_001454.2:n.797+153A>T
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