Canonical Allele Identifier: CA350942

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12658113C>A , CM000681.2:g.12658113C>A	GRCh38
NC_000019.9:g.12768927C>A , CM000681.1:g.12768927C>A	GRCh37
NC_000019.8:g.12629927C>A	NCBI36
NG_008318.1:g.13665G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000528.4:c.1259G>T MANE Select	NP_000519.2:p.Gly420Val
ENST00000456935.7:c.1259G>T MANE Select	ENSP00000395473.2:p.Gly420Val
NM_000528.3:c.1259G>T	NP_000519.2:p.Gly420Val
NM_001173498.1:c.1256G>T	NP_001166969.1:p.Gly419Val
NM_001173498.2:c.1256G>T	NP_001166969.1:p.Gly419Val
ENST00000221363.8:c.1256G>T	ENSP00000221363.4:p.Gly419Val
ENST00000456935.6:c.1259G>T	ENSP00000395473.2:p.Gly420Val
ENST00000465830.1:n.423G>T
ENST00000466794.5:n.1158G>T
ENST00000495617.1:n.281-353G>T
XM_005259913.1:c.1262G>T	XP_005259970.1:p.Gly421Val
XM_005259913.2:c.1262G>T	XP_005259970.1:p.Gly421Val
XM_011528017.1:c.158G>T	XP_011526319.1:p.Gly53Val
XM_024451518.1:c.158G>T	XP_024307286.1:p.Gly53Val