Canonical Allele Identifier: CA920061331

Gene: MAN2B1

Linked Data

• dbSNP Id: rs1568298588

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12649332del , CM000681.2:g.12649332del	GRCh38
NC_000019.9:g.12760146del , CM000681.1:g.12760146del	GRCh37
NC_000019.8:g.12621146del	NCBI36
NG_008318.1:g.22450del

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.2355+13del MANE Select	ENSP00000395473.2:n.2355+13del
ENST00000221363.8:c.2352+13del	ENSP00000221363.4:n.2352+13del
ENST00000456935.6:c.2355+13del	ENSP00000395473.2:n.2355+13del
ENST00000466794.5:n.2945+13del
NM_000528.3:c.2355+13del	NP_000519.2:n.2355+13del
NM_001173498.1:c.2352+13del	NP_001166969.1:n.2352+13del
XM_005259913.1:c.2358+13del	XP_005259970.1:n.2358+13del
XM_011528017.1:c.1254+13del	XP_011526319.1:n.1254+13del
XM_005259913.2:c.2358+13del	XP_005259970.1:n.2358+13del
XM_024451518.1:c.1254+13del	XP_024307286.1:n.1254+13del
NM_000528.4:c.2355+13del MANE Select	NP_000519.2:n.2355+13del
NM_001173498.2:c.2352+13del	NP_001166969.1:n.2352+13del