Canonical Allele Identifier: CA430432242
Gene: FRZB HGNC NCBI

Linked Data

dbSNP Id: rs1695553899
MyVariant Identifiers: chr2:g.183703334C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838606C>T , CM000664.2:g.182838606C>T GRCh38
NC_000002.11:g.183703334C>T , CM000664.1:g.183703334C>T GRCh37
NC_000002.10:g.183411579C>T NCBI36
NG_017197.1:g.33165G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.600G>A MANE Select ENSP00000295113.4:p.Arg200=
ENST00000295113.4:c.600G>A ENSP00000295113.4:p.Arg200=
NM_001463.3:c.600G>A NP_001454.2:p.Arg200=
NM_001463.4:c.600G>A MANE Select NP_001454.2:p.Arg200=
Search 100 bp 5'
Search 100 bp 3'