Canonical Allele Identifier: CA2323507821
Gene: MAN2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12665679G= , CM000681.2:g.12665679G= GRCh38
NC_000019.9:g.12776493G= , CM000681.1:g.12776493G= GRCh37
NC_000019.8:g.12637493G= NCBI36
NG_008318.1:g.6099C=
NG_015814.1:g.3876G=

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.262+24C= MANE Select ENSP00000395473.2:n.262+24C=
ENST00000221363.8:c.262+24C= ENSP00000221363.4:n.262+24C=
ENST00000456935.6:c.262+24C= ENSP00000395473.2:n.262+24C=
ENST00000466794.5:n.244+24C=
ENST00000486847.2:c.160-154C= ENSP00000470174.1:n.160-154C=
ENST00000596512.5:n.201-154C=
ENST00000597961.1:c.253+24C= ENSP00000472710.1:n.253+24C=
ENST00000598876.1:c.289+24C= ENSP00000470533.1:n.289+24C=
ENST00000600281.1:n.303+24C=
NM_000528.3:c.262+24C= NP_000519.2:n.262+24C=
NM_001173498.1:c.262+24C= NP_001166969.1:n.262+24C=
XM_005259913.1:c.262+24C= XP_005259970.1:n.262+24C=
XM_005259913.2:c.262+24C= XP_005259970.1:n.262+24C=
XM_024451518.1:c.-757+24C= XP_024307286.1:n.-757+24C=
NM_000528.4:c.262+24C= MANE Select NP_000519.2:n.262+24C=
NM_001173498.2:c.262+24C= NP_001166969.1:n.262+24C=