Canonical Allele Identifier: CA408920652
Gene: CHMP4B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33851066G>C , CM000682.2:g.33851066G>C GRCh38
NC_000020.10:g.32438872G>C , CM000682.1:g.32438872G>C GRCh37
NC_000020.9:g.31902533G>C NCBI36
NG_015820.1:g.44763G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000217402.3:c.483G>C MANE Select ENSP00000217402.2:p.Glu161Asp
ENST00000217402.2:c.483G>C ENSP00000217402.2:p.Glu161Asp
NM_176812.4:c.483G>C NP_789782.1:p.Glu161Asp
NM_176812.5:c.483G>C MANE Select NP_789782.1:p.Glu161Asp