Canonical Allele Identifier: CA408920456
Gene: CHMP4B HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.32438787A>C (hg19) chr20:g.33850981A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33850981A>C , CM000682.2:g.33850981A>C GRCh38
NC_000020.10:g.32438787A>C , CM000682.1:g.32438787A>C GRCh37
NC_000020.9:g.31902448A>C NCBI36
NG_015820.1:g.44678A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000217402.3:c.398A>C MANE Select ENSP00000217402.2:p.Gln133Pro
ENST00000217402.2:c.398A>C ENSP00000217402.2:p.Gln133Pro
NM_176812.4:c.398A>C NP_789782.1:p.Gln133Pro
NM_176812.5:c.398A>C MANE Select NP_789782.1:p.Gln133Pro
Search 100 bp 5'
Search 100 bp 3'