Canonical Allele Identifier: CA2360938941
Gene: CHMP4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33850987T= , CM000682.2:g.33850987T= GRCh38
NC_000020.10:g.32438793T= , CM000682.1:g.32438793T= GRCh37
NC_000020.9:g.31902454T= NCBI36
NG_015820.1:g.44684T=

Transcript Alleles

HGVS Amino-acid change
ENST00000217402.3:c.404T= MANE Select ENSP00000217402.2:p.Ile135=
ENST00000217402.2:c.404T= ENSP00000217402.2:p.Ile135=
NM_176812.4:c.404T= NP_789782.1:p.Ile135=
NM_176812.5:c.404T= MANE Select NP_789782.1:p.Ile135=