Canonical Allele Identifier: CA1500302210
Gene: FREM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.143695233C= , CM000666.2:g.143695233C= GRCh38
NC_000004.11:g.144616386C= , CM000666.1:g.144616386C= GRCh37
NC_000004.10:g.144835836C= NCBI36
NG_052820.1:g.10443G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329798.5:c.5185+258G= MANE Select ENSP00000332886.5:n.5185+258G=
NM_001168235.1:c.5185+258G= NP_001161707.1:n.5185+258G=
NM_001168235.2:c.5185+258G= MANE Select NP_001161707.1:n.5185+258G=