Canonical Allele Identifier: CA408920648
Gene: CHMP4B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33851064G>T , CM000682.2:g.33851064G>T GRCh38
NC_000020.10:g.32438870G>T , CM000682.1:g.32438870G>T GRCh37
NC_000020.9:g.31902531G>T NCBI36
NG_015820.1:g.44761G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000217402.3:c.481G>T MANE Select ENSP00000217402.2:p.Glu161Ter
ENST00000217402.2:c.481G>T ENSP00000217402.2:p.Glu161Ter
NM_176812.4:c.481G>T NP_789782.1:p.Glu161Ter
NM_176812.5:c.481G>T MANE Select NP_789782.1:p.Glu161Ter