Canonical Allele Identifier: CA2763853698

Gene: FREM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.143695239T>C , CM000666.2:g.143695239T>C	GRCh38
NC_000004.11:g.144616392T>C , CM000666.1:g.144616392T>C	GRCh37
NC_000004.10:g.144835842T>C	NCBI36
NG_052820.1:g.10437A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000329798.5:c.5185+252A>G MANE Select	ENSP00000332886.5:n.5185+252A>G
NM_001168235.1:c.5185+252A>G	NP_001161707.1:n.5185+252A>G
NM_001168235.2:c.5185+252A>G MANE Select	NP_001161707.1:n.5185+252A>G