Canonical Allele Identifier: CA430432156
Gene: FRZB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.183703289T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838561T>G , CM000664.2:g.182838561T>G GRCh38
NC_000002.11:g.183703289T>G , CM000664.1:g.183703289T>G GRCh37
NC_000002.10:g.183411534T>G NCBI36
NG_017197.1:g.33210A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.645A>C MANE Select ENSP00000295113.4:p.Ala215=
ENST00000295113.4:c.645A>C ENSP00000295113.4:p.Ala215=
NM_001463.3:c.645A>C NP_001454.2:p.Ala215=
NM_001463.4:c.645A>C MANE Select NP_001454.2:p.Ala215=
Search 100 bp 5'
Search 100 bp 3'