Canonical Allele Identifier: CA1500302206
Gene: FREM3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.143695226G= , CM000666.2:g.143695226G= GRCh38
NC_000004.11:g.144616379G= , CM000666.1:g.144616379G= GRCh37
NC_000004.10:g.144835829G= NCBI36
NG_052820.1:g.10450C=

Transcript Alleles

HGVS Amino-acid change
ENST00000329798.5:c.5185+265C= MANE Select ENSP00000332886.5:n.5185+265C=
NM_001168235.1:c.5185+265C= NP_001161707.1:n.5185+265C=
NM_001168235.2:c.5185+265C= MANE Select NP_001161707.1:n.5185+265C=
Search 100 bp 5'
Search 100 bp 3'