Canonical Allele Identifier: CA1500258050
Gene: FREM3 HGNC NCBI
GUSBP5 HGNC NCBI

Linked Data

dbSNP Id: rs1738166869
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.143582536A>T , CM000666.2:g.143582536A>T GRCh38
NC_000004.11:g.144503689A>T , CM000666.1:g.144503689A>T GRCh37
NC_000004.10:g.144723139A>T NCBI36
NG_052820.1:g.123140T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000329798.5:c.6178+3308T>A (FREM3) MANE Select ENSP00000332886.5:n.6178+3308T>A
ENST00000511042.5:n.191+9955A>T (GUSBP5)
NM_001168235.1:c.6178+3308T>A (FREM3) NP_001161707.1:n.6178+3308T>A
NM_001168235.2:c.6178+3308T>A (FREM3) MANE Select NP_001161707.1:n.6178+3308T>A
Search 100 bp 5'
Search 100 bp 3'