Canonical Allele Identifier: CA2707506797
Gene: FREM3 HGNC NCBI
GUSBP5 HGNC NCBI

Linked Data

dbSNP Id: rs2149832847

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.143582557T>C , CM000666.2:g.143582557T>C GRCh38
NC_000004.11:g.144503710T>C , CM000666.1:g.144503710T>C GRCh37
NC_000004.10:g.144723160T>C NCBI36
NG_052820.1:g.123119A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000329798.5:c.6178+3287A>G (FREM3) MANE Select ENSP00000332886.5:n.6178+3287A>G
ENST00000511042.5:n.191+9976T>C (GUSBP5)
NM_001168235.1:c.6178+3287A>G (FREM3) NP_001161707.1:n.6178+3287A>G
NM_001168235.2:c.6178+3287A>G (FREM3) MANE Select NP_001161707.1:n.6178+3287A>G