Canonical Allele Identifier: CA2662236391
Gene: FRZB HGNC NCBI

Linked Data

gnomAD v4: 2-182838339-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838339C>T , CM000664.2:g.182838339C>T GRCh38
NC_000002.11:g.183703067C>T , CM000664.1:g.183703067C>T GRCh37
NC_000002.10:g.183411312C>T NCBI36
NG_017197.1:g.33432G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.797+70G>A MANE Select ENSP00000295113.4:n.797+70G>A
ENST00000295113.4:c.797+70G>A ENSP00000295113.4:n.797+70G>A
NM_001463.3:c.797+70G>A NP_001454.2:n.797+70G>A
NM_001463.4:c.797+70G>A MANE Select NP_001454.2:n.797+70G>A
Search 100 bp 5'
Search 100 bp 3'