Canonical Allele Identifier: CA2360938978
Gene: CHMP4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33851101A= , CM000682.2:g.33851101A= GRCh38
NC_000020.10:g.32438907A= , CM000682.1:g.32438907A= GRCh37
NC_000020.9:g.31902568A= NCBI36
NG_015820.1:g.44798A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217402.3:c.483+35A= MANE Select ENSP00000217402.2:n.483+35A=
ENST00000217402.2:c.483+35A= ENSP00000217402.2:n.483+35A=
NM_176812.4:c.483+35A= NP_789782.1:n.483+35A=
NM_176812.5:c.483+35A= MANE Select NP_789782.1:n.483+35A=