Canonical Allele Identifier: CA305460544

Gene: MAN2B1

Linked Data

• dbSNP Id: rs976021105
• gnomAD v2: 19-12758528-AG-A
• gnomAD v3: 19-12647714-AG-A
• gnomAD v4: 19-12647714-AG-A
• MyVariant Identifiers: chr19:g.12758529del (hg19) ; chr19:g.12647715del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647718del , CM000681.2:g.12647718del	GRCh38
NC_000019.9:g.12758532del , CM000681.1:g.12758532del	GRCh37
NC_000019.8:g.12619532del	NCBI36
NG_008318.1:g.24063del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2665-117del MANE Select	ENSP00000395473.2:n.2665-117del
ENST00000221363.8:c.2662-117del	ENSP00000221363.4:n.2662-117del
ENST00000456935.6:c.2665-117del	ENSP00000395473.2:n.2665-117del
ENST00000466794.5:n.3255-117del
ENST00000597692.1:c.224-117del
NM_000528.3:c.2665-117del	NP_000519.2:n.2665-117del
NM_001173498.1:c.2662-117del	NP_001166969.1:n.2662-117del
XM_005259913.1:c.2668-117del	XP_005259970.1:n.2668-117del
XM_011528017.1:c.1564-117del	XP_011526319.1:n.1564-117del
XM_005259913.2:c.2668-117del	XP_005259970.1:n.2668-117del
XM_024451518.1:c.1564-117del	XP_024307286.1:n.1564-117del
NM_000528.4:c.2665-117del MANE Select	NP_000519.2:n.2665-117del
NM_001173498.2:c.2662-117del	NP_001166969.1:n.2662-117del