Canonical Allele Identifier: CA1500302222
Gene: FREM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.143695251G= , CM000666.2:g.143695251G= GRCh38
NC_000004.11:g.144616404G= , CM000666.1:g.144616404G= GRCh37
NC_000004.10:g.144835854G= NCBI36
NG_052820.1:g.10425C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329798.5:c.5185+240C= MANE Select ENSP00000332886.5:n.5185+240C=
NM_001168235.1:c.5185+240C= NP_001161707.1:n.5185+240C=
NM_001168235.2:c.5185+240C= MANE Select NP_001161707.1:n.5185+240C=