Canonical Allele Identifier: CA349750443
Gene: FRZB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.183703209C>T (hg19) chr2:g.182838481C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838481C>T , CM000664.2:g.182838481C>T GRCh38
NC_000002.11:g.183703209C>T , CM000664.1:g.183703209C>T GRCh37
NC_000002.10:g.183411454C>T NCBI36
NG_017197.1:g.33290G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.725G>A MANE Select ENSP00000295113.4:p.Gly242Asp
ENST00000295113.4:c.725G>A ENSP00000295113.4:p.Gly242Asp
NM_001463.3:c.725G>A NP_001454.2:p.Gly242Asp
NM_001463.4:c.725G>A MANE Select NP_001454.2:p.Gly242Asp
Search 100 bp 5'
Search 100 bp 3'