Canonical Allele Identifier: CA920061303
Gene: MAN2B1 HGNC NCBI

Linked Data

dbSNP Id: rs1568297035

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12647284_12647377dup , CM000681.2:g.12647284_12647377dup GRCh38
NC_000019.9:g.12758098_12758191dup , CM000681.1:g.12758098_12758191dup GRCh37
NC_000019.8:g.12619098_12619191dup NCBI36
NG_008318.1:g.24401_24494dup

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.2821-42_2872dup
ENST00000221363.8:c.2818-42_2869dup
ENST00000456935.6:c.2821-42_2872dup
ENST00000466794.5:n.3411-42_3462dup
ENST00000469423.1:n.208_301dup
ENST00000493218.5:n.232-42_283dup
ENST00000597692.1:c.380-42_431dup
NM_000528.3:c.2821-42_2872dup
NM_001173498.1:c.2818-42_2869dup
XM_005259913.1:c.2824-42_2875dup
XM_011528017.1:c.1720-42_1771dup
XM_005259913.2:c.2824-42_2875dup
XM_024451518.1:c.1720-42_1771dup
NM_000528.4:c.2821-42_2872dup
NM_001173498.2:c.2818-42_2869dup