Canonical Allele Identifier: CA1500302226
Gene: FREM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.143695256A= , CM000666.2:g.143695256A= GRCh38
NC_000004.11:g.144616409A= , CM000666.1:g.144616409A= GRCh37
NC_000004.10:g.144835859A= NCBI36
NG_052820.1:g.10420T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329798.5:c.5185+235T= MANE Select ENSP00000332886.5:n.5185+235T=
NM_001168235.1:c.5185+235T= NP_001161707.1:n.5185+235T=
NM_001168235.2:c.5185+235T= MANE Select NP_001161707.1:n.5185+235T=