Canonical Allele Identifier: CA408920651
Gene: CHMP4B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33851065A>T , CM000682.2:g.33851065A>T GRCh38
NC_000020.10:g.32438871A>T , CM000682.1:g.32438871A>T GRCh37
NC_000020.9:g.31902532A>T NCBI36
NG_015820.1:g.44762A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000217402.3:c.482A>T MANE Select ENSP00000217402.2:p.Glu161Val
ENST00000217402.2:c.482A>T ENSP00000217402.2:p.Glu161Val
NM_176812.4:c.482A>T NP_789782.1:p.Glu161Val
NM_176812.5:c.482A>T MANE Select NP_789782.1:p.Glu161Val