Canonical Allele Identifier: CA1500302246
Gene: FREM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.143695272A= , CM000666.2:g.143695272A= GRCh38
NC_000004.11:g.144616425A= , CM000666.1:g.144616425A= GRCh37
NC_000004.10:g.144835875A= NCBI36
NG_052820.1:g.10404T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329798.5:c.5185+219T= MANE Select ENSP00000332886.5:n.5185+219T=
NM_001168235.1:c.5185+219T= NP_001161707.1:n.5185+219T=
NM_001168235.2:c.5185+219T= MANE Select NP_001161707.1:n.5185+219T=