Canonical Allele Identifier: CA1312515782

Gene: FRZB

Linked Data

• dbSNP Id: rs1695549273

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.182838271C>G , CM000664.2:g.182838271C>G	GRCh38
NC_000002.11:g.183702999C>G , CM000664.1:g.183702999C>G	GRCh37
NC_000002.10:g.183411244C>G	NCBI36
NG_017197.1:g.33500G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295113.5:c.797+138G>C MANE Select	ENSP00000295113.4:n.797+138G>C
ENST00000295113.4:c.797+138G>C	ENSP00000295113.4:n.797+138G>C
NM_001463.3:c.797+138G>C	NP_001454.2:n.797+138G>C
NM_001463.4:c.797+138G>C MANE Select	NP_001454.2:n.797+138G>C