Canonical Allele Identifier: CA1500302138
Gene: FREM3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.143695140T= , CM000666.2:g.143695140T= GRCh38
NC_000004.11:g.144616293T= , CM000666.1:g.144616293T= GRCh37
NC_000004.10:g.144835743T= NCBI36
NG_052820.1:g.10536A=

Transcript Alleles

HGVS Amino-acid change
ENST00000329798.5:c.5185+351A= MANE Select ENSP00000332886.5:n.5185+351A=
NM_001168235.1:c.5185+351A= NP_001161707.1:n.5185+351A=
NM_001168235.2:c.5185+351A= MANE Select NP_001161707.1:n.5185+351A=
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