Canonical Allele Identifier: CA313391166
Gene: CHMP4B HGNC NCBI

Linked Data

dbSNP Id: rs886298704
MyVariant Identifiers: chr20:g.32438899A>G (hg19) chr20:g.33851093A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33851093A>G , CM000682.2:g.33851093A>G GRCh38
NC_000020.10:g.32438899A>G , CM000682.1:g.32438899A>G GRCh37
NC_000020.9:g.31902560A>G NCBI36
NG_015820.1:g.44790A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000217402.3:c.483+27A>G MANE Select ENSP00000217402.2:n.483+27A>G
ENST00000217402.2:c.483+27A>G ENSP00000217402.2:n.483+27A>G
NM_176812.4:c.483+27A>G NP_789782.1:n.483+27A>G
NM_176812.5:c.483+27A>G MANE Select NP_789782.1:n.483+27A>G
Search 100 bp 5'
Search 100 bp 3'