Canonical Allele Identifier: CA2577180413
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838367A>C , CM000664.2:g.182838367A>C GRCh38
NC_000002.11:g.183703095A>C , CM000664.1:g.183703095A>C GRCh37
NC_000002.10:g.183411340A>C NCBI36
NG_017197.1:g.33404T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.797+42T>G MANE Select ENSP00000295113.4:n.797+42T>G
ENST00000295113.4:c.797+42T>G ENSP00000295113.4:n.797+42T>G
NM_001463.3:c.797+42T>G NP_001454.2:n.797+42T>G
NM_001463.4:c.797+42T>G MANE Select NP_001454.2:n.797+42T>G