Canonical Allele Identifier: CA408920657
Gene: CHMP4B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33851068T>A , CM000682.2:g.33851068T>A GRCh38
NC_000020.10:g.32438874T>A , CM000682.1:g.32438874T>A GRCh37
NC_000020.9:g.31902535T>A NCBI36
NG_015820.1:g.44765T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000217402.3:c.483+2T>A MANE Select ENSP00000217402.2:n.483+2T>A
ENST00000217402.2:c.483+2T>A ENSP00000217402.2:n.483+2T>A
NM_176812.4:c.483+2T>A NP_789782.1:n.483+2T>A
NM_176812.5:c.483+2T>A MANE Select NP_789782.1:n.483+2T>A