Canonical Allele Identifier: CA9819963
Gene: CHMP4B HGNC NCBI

Linked Data

dbSNP Id: rs745999954

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33851101A>G , CM000682.2:g.33851101A>G GRCh38
NC_000020.10:g.32438907A>G , CM000682.1:g.32438907A>G GRCh37
NC_000020.9:g.31902568A>G NCBI36
NG_015820.1:g.44798A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217402.3:c.483+35A>G MANE Select ENSP00000217402.2:n.483+35A>G
ENST00000217402.2:c.483+35A>G ENSP00000217402.2:n.483+35A>G
NM_176812.4:c.483+35A>G NP_789782.1:n.483+35A>G
NM_176812.5:c.483+35A>G MANE Select NP_789782.1:n.483+35A>G