Canonical Allele Identifier: CA761677518
Gene: FRZB HGNC NCBI

Linked Data

dbSNP Id: rs1183058223
MyVariant Identifiers: chr2:g.183703082T>C (hg19) chr2:g.182838354T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838354T>C , CM000664.2:g.182838354T>C GRCh38
NC_000002.11:g.183703082T>C , CM000664.1:g.183703082T>C GRCh37
NC_000002.10:g.183411327T>C NCBI36
NG_017197.1:g.33417A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.797+55A>G MANE Select ENSP00000295113.4:n.797+55A>G
ENST00000295113.4:c.797+55A>G ENSP00000295113.4:n.797+55A>G
NM_001463.3:c.797+55A>G NP_001454.2:n.797+55A>G
NM_001463.4:c.797+55A>G MANE Select NP_001454.2:n.797+55A>G
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