Canonical Allele Identifier: CA2360938942
Gene: CHMP4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33850992G= , CM000682.2:g.33850992G= GRCh38
NC_000020.10:g.32438798G= , CM000682.1:g.32438798G= GRCh37
NC_000020.9:g.31902459G= NCBI36
NG_015820.1:g.44689G=

Transcript Alleles

HGVS Amino-acid change
ENST00000217402.3:c.409G= MANE Select ENSP00000217402.2:p.Asp137=
ENST00000217402.2:c.409G= ENSP00000217402.2:p.Asp137=
NM_176812.4:c.409G= NP_789782.1:p.Asp137=
NM_176812.5:c.409G= MANE Select NP_789782.1:p.Asp137=