Canonical Allele Identifier: CA1500212326
Gene: FREM3 HGNC NCBI
GUSBP5 HGNC NCBI

Linked Data

dbSNP Id: rs1578821893

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.143587585A>G , CM000666.2:g.143587585A>G GRCh38
NC_000004.11:g.144508738A>G , CM000666.1:g.144508738A>G GRCh37
NC_000004.10:g.144728188A>G NCBI36
NG_052820.1:g.118091T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000329798.5:c.6029-1592T>C (FREM3) MANE Select ENSP00000332886.5:n.6029-1592T>C
ENST00000511042.5:n.191+15004A>G (GUSBP5)
NM_001168235.1:c.6029-1592T>C (FREM3) NP_001161707.1:n.6029-1592T>C
NM_001168235.2:c.6029-1592T>C (FREM3) MANE Select NP_001161707.1:n.6029-1592T>C