Canonical Allele Identifier: CA510407258
Gene: CHMP4B HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.32438797T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33850991T>A , CM000682.2:g.33850991T>A GRCh38
NC_000020.10:g.32438797T>A , CM000682.1:g.32438797T>A GRCh37
NC_000020.9:g.31902458T>A NCBI36
NG_015820.1:g.44688T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000217402.3:c.408T>A MANE Select ENSP00000217402.2:p.Ala136=
ENST00000217402.2:c.408T>A ENSP00000217402.2:p.Ala136=
NM_176812.4:c.408T>A NP_789782.1:p.Ala136=
NM_176812.5:c.408T>A MANE Select NP_789782.1:p.Ala136=
Search 100 bp 5'
Search 100 bp 3'