Canonical Allele Identifier: CA106878349
Gene: FREM3 HGNC NCBI

Linked Data

dbSNP Id: rs1034978697
MyVariant Identifiers: chr4:g.144616418T>C (hg19) chr4:g.143695265T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.143695265T>C , CM000666.2:g.143695265T>C GRCh38
NC_000004.11:g.144616418T>C , CM000666.1:g.144616418T>C GRCh37
NC_000004.10:g.144835868T>C NCBI36
NG_052820.1:g.10411A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000329798.5:c.5185+226A>G MANE Select ENSP00000332886.5:n.5185+226A>G
NM_001168235.1:c.5185+226A>G NP_001161707.1:n.5185+226A>G
NM_001168235.2:c.5185+226A>G MANE Select NP_001161707.1:n.5185+226A>G
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