Canonical Allele Identifier: CA2582722023

Gene: MAN2B1

Linked Data

• gnomAD v4: 19-12663295-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12663295A>G , CM000681.2:g.12663295A>G	GRCh38
NC_000019.9:g.12774109A>G , CM000681.1:g.12774109A>G	GRCh37
NC_000019.8:g.12635109A>G	NCBI36
NG_008318.1:g.8483T>C
NG_015814.1:g.1492A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.909+22T>C MANE Select	ENSP00000395473.2:n.909+22T>C
ENST00000221363.8:c.909+22T>C	ENSP00000221363.4:n.909+22T>C
ENST00000456935.6:c.909+22T>C	ENSP00000395473.2:n.909+22T>C
ENST00000462144.1:n.102+22T>C
ENST00000466794.5:n.891+22T>C
NM_000528.3:c.909+22T>C	NP_000519.2:n.909+22T>C
NM_001173498.1:c.909+22T>C	NP_001166969.1:n.909+22T>C
XM_005259913.1:c.909+22T>C	XP_005259970.1:n.909+22T>C
XM_011528017.1:c.-110+22T>C	XP_011526319.1:n.-110+22T>C
XM_005259913.2:c.909+22T>C	XP_005259970.1:n.909+22T>C
XM_024451518.1:c.-110+22T>C	XP_024307286.1:n.-110+22T>C
NM_000528.4:c.909+22T>C MANE Select	NP_000519.2:n.909+22T>C
NM_001173498.2:c.909+22T>C	NP_001166969.1:n.909+22T>C