Canonical Allele Identifier: CA510407270
Gene: CHMP4B HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.32438800C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33850994C>T , CM000682.2:g.33850994C>T GRCh38
NC_000020.10:g.32438800C>T , CM000682.1:g.32438800C>T GRCh37
NC_000020.9:g.31902461C>T NCBI36
NG_015820.1:g.44691C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000217402.3:c.411C>T MANE Select ENSP00000217402.2:p.Asp137=
ENST00000217402.2:c.411C>T ENSP00000217402.2:p.Asp137=
NM_176812.4:c.411C>T NP_789782.1:p.Asp137=
NM_176812.5:c.411C>T MANE Select NP_789782.1:p.Asp137=
Search 100 bp 5'
Search 100 bp 3'