Canonical Allele Identifier: CA404237810

Gene: MAN2B1

Linked Data

• gnomAD v4: 19-12647489-T-A
• MyVariant Identifiers: chr19:g.12758303T>A (hg19) ; chr19:g.12647489T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647489T>A , CM000681.2:g.12647489T>A	GRCh38
NC_000019.9:g.12758303T>A , CM000681.1:g.12758303T>A	GRCh37
NC_000019.8:g.12619303T>A	NCBI36
NG_008318.1:g.24289A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.2774A>T MANE Select	ENSP00000395473.2:p.Glu925Val
ENST00000221363.8:c.2771A>T	ENSP00000221363.4:p.Glu924Val
ENST00000456935.6:c.2774A>T	ENSP00000395473.2:p.Glu925Val
ENST00000466794.5:n.3364A>T
ENST00000469423.1:n.96A>T
ENST00000493218.5:n.185A>T
ENST00000597692.1:c.333A>T
NM_000528.3:c.2774A>T	NP_000519.2:p.Glu925Val
NM_001173498.1:c.2771A>T	NP_001166969.1:p.Glu924Val
XM_005259913.1:c.2777A>T	XP_005259970.1:p.Glu926Val
XM_011528017.1:c.1673A>T	XP_011526319.1:p.Glu558Val
XM_005259913.2:c.2777A>T	XP_005259970.1:p.Glu926Val
XM_024451518.1:c.1673A>T	XP_024307286.1:p.Glu558Val
NM_000528.4:c.2774A>T MANE Select	NP_000519.2:p.Glu925Val
NM_001173498.2:c.2771A>T	NP_001166969.1:p.Glu924Val