Canonical Allele Identifier: CA1500302198
Gene: FREM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.143695213A= , CM000666.2:g.143695213A= GRCh38
NC_000004.11:g.144616366A= , CM000666.1:g.144616366A= GRCh37
NC_000004.10:g.144835816A= NCBI36
NG_052820.1:g.10463T=

Transcript Alleles

HGVS Amino-acid change
ENST00000329798.5:c.5185+278T= MANE Select ENSP00000332886.5:n.5185+278T=
NM_001168235.1:c.5185+278T= NP_001161707.1:n.5185+278T=
NM_001168235.2:c.5185+278T= MANE Select NP_001161707.1:n.5185+278T=