Canonical Allele Identifier: CA1500302218
Gene: FREM3 HGNC NCBI

Linked Data

dbSNP Id: rs1740543383
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.143695246T>G , CM000666.2:g.143695246T>G GRCh38
NC_000004.11:g.144616399T>G , CM000666.1:g.144616399T>G GRCh37
NC_000004.10:g.144835849T>G NCBI36
NG_052820.1:g.10430A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000329798.5:c.5185+245A>C MANE Select ENSP00000332886.5:n.5185+245A>C
NM_001168235.1:c.5185+245A>C NP_001161707.1:n.5185+245A>C
NM_001168235.2:c.5185+245A>C MANE Select NP_001161707.1:n.5185+245A>C
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