Canonical Allele Identifier: CA2582717944
Gene: MAN2B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12649136del , CM000681.2:g.12649136del GRCh38
NC_000019.9:g.12759950del , CM000681.1:g.12759950del GRCh37
NC_000019.8:g.12620950del NCBI36
NG_008318.1:g.22643del

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.2436+1del
ENST00000221363.8:c.2433+1del
ENST00000456935.6:c.2436+1del
ENST00000466794.5:n.3026+1del
NM_000528.3:c.2436+1del
NM_001173498.1:c.2433+1del
XM_005259913.1:c.2439+1del
XM_011528017.1:c.1335+1del
XM_005259913.2:c.2439+1del
XM_024451518.1:c.1335+1del
NM_000528.4:c.2436+1del
NM_001173498.2:c.2433+1del