Canonical Allele Identifier: CA761677496

Gene: FRZB

Linked Data

• dbSNP Id: rs1199628466
• gnomAD v3: 2-182838235-C-T
• gnomAD v4: 2-182838235-C-T
• MyVariant Identifiers: chr2:g.183702963C>T (hg19) ; chr2:g.182838235C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.182838235C>T , CM000664.2:g.182838235C>T	GRCh38
NC_000002.11:g.183702963C>T , CM000664.1:g.183702963C>T	GRCh37
NC_000002.10:g.183411208C>T	NCBI36
NG_017197.1:g.33536G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295113.5:c.797+174G>A MANE Select	ENSP00000295113.4:n.797+174G>A
ENST00000295113.4:c.797+174G>A	ENSP00000295113.4:n.797+174G>A
NM_001463.3:c.797+174G>A	NP_001454.2:n.797+174G>A
NM_001463.4:c.797+174G>A MANE Select	NP_001454.2:n.797+174G>A