Canonical Allele Identifier: CA743757274
Gene: CHMP4B HGNC NCBI

Linked Data

dbSNP Id: rs1211033402
gnomAD v3: 20-33850900-C-T
gnomAD v4: 20-33850900-C-T
MyVariant Identifiers: chr20:g.32438706C>T (hg19) chr20:g.33850900C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33850900C>T , CM000682.2:g.33850900C>T GRCh38
NC_000020.10:g.32438706C>T , CM000682.1:g.32438706C>T GRCh37
NC_000020.9:g.31902367C>T NCBI36
NG_015820.1:g.44597C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000217402.3:c.369-52C>T MANE Select ENSP00000217402.2:n.369-52C>T
ENST00000217402.2:c.369-52C>T ENSP00000217402.2:n.369-52C>T
NM_176812.4:c.369-52C>T NP_789782.1:n.369-52C>T
NM_176812.5:c.369-52C>T MANE Select NP_789782.1:n.369-52C>T
Search 100 bp 5'
Search 100 bp 3'