Canonical Allele Identifier: CA635517159
Gene: CHMP4B HGNC NCBI

Linked Data

dbSNP Id: rs1381674114

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33851103A>G , CM000682.2:g.33851103A>G GRCh38
NC_000020.10:g.32438909A>G , CM000682.1:g.32438909A>G GRCh37
NC_000020.9:g.31902570A>G NCBI36
NG_015820.1:g.44800A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217402.3:c.483+37A>G MANE Select ENSP00000217402.2:n.483+37A>G
ENST00000217402.2:c.483+37A>G ENSP00000217402.2:n.483+37A>G
NM_176812.4:c.483+37A>G NP_789782.1:n.483+37A>G
NM_176812.5:c.483+37A>G MANE Select NP_789782.1:n.483+37A>G