Canonical Allele Identifier: CA2763853697
Gene: FREM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.143695228C>G , CM000666.2:g.143695228C>G GRCh38
NC_000004.11:g.144616381C>G , CM000666.1:g.144616381C>G GRCh37
NC_000004.10:g.144835831C>G NCBI36
NG_052820.1:g.10448G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000329798.5:c.5185+263G>C MANE Select ENSP00000332886.5:n.5185+263G>C
NM_001168235.1:c.5185+263G>C NP_001161707.1:n.5185+263G>C
NM_001168235.2:c.5185+263G>C MANE Select NP_001161707.1:n.5185+263G>C