Canonical Allele Identifier: CA408920484
Gene: CHMP4B HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.32438799A>C (hg19) chr20:g.33850993A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33850993A>C , CM000682.2:g.33850993A>C GRCh38
NC_000020.10:g.32438799A>C , CM000682.1:g.32438799A>C GRCh37
NC_000020.9:g.31902460A>C NCBI36
NG_015820.1:g.44690A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000217402.3:c.410A>C MANE Select ENSP00000217402.2:p.Asp137Ala
ENST00000217402.2:c.410A>C ENSP00000217402.2:p.Asp137Ala
NM_176812.4:c.410A>C NP_789782.1:p.Asp137Ala
NM_176812.5:c.410A>C MANE Select NP_789782.1:p.Asp137Ala
Search 100 bp 5'
Search 100 bp 3'