Canonical Allele Identifier: CA635517155
Gene: CHMP4B HGNC NCBI

Linked Data

dbSNP Id: rs1392668811
gnomAD v2: 20-32438892-T-A
gnomAD v4: 20-33851086-T-A
MyVariant Identifiers: chr20:g.32438892T>A (hg19) chr20:g.33851086T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33851086T>A , CM000682.2:g.33851086T>A GRCh38
NC_000020.10:g.32438892T>A , CM000682.1:g.32438892T>A GRCh37
NC_000020.9:g.31902553T>A NCBI36
NG_015820.1:g.44783T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000217402.3:c.483+20T>A MANE Select ENSP00000217402.2:n.483+20T>A
ENST00000217402.2:c.483+20T>A ENSP00000217402.2:n.483+20T>A
NM_176812.4:c.483+20T>A NP_789782.1:n.483+20T>A
NM_176812.5:c.483+20T>A MANE Select NP_789782.1:n.483+20T>A
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