Canonical Allele Identifier: CA404237845

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12758312G>T (hg19) ; chr19:g.12647498G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647498G>T , CM000681.2:g.12647498G>T	GRCh38
NC_000019.9:g.12758312G>T , CM000681.1:g.12758312G>T	GRCh37
NC_000019.8:g.12619312G>T	NCBI36
NG_008318.1:g.24280C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2765C>A MANE Select	ENSP00000395473.2:p.Ala922Asp
ENST00000221363.8:c.2762C>A	ENSP00000221363.4:p.Ala921Asp
ENST00000456935.6:c.2765C>A	ENSP00000395473.2:p.Ala922Asp
ENST00000466794.5:n.3355C>A
ENST00000469423.1:n.87C>A
ENST00000493218.5:n.176C>A
ENST00000597692.1:c.324C>A
NM_000528.3:c.2765C>A	NP_000519.2:p.Ala922Asp
NM_001173498.1:c.2762C>A	NP_001166969.1:p.Ala921Asp
XM_005259913.1:c.2768C>A	XP_005259970.1:p.Ala923Asp
XM_011528017.1:c.1664C>A	XP_011526319.1:p.Ala555Asp
XM_005259913.2:c.2768C>A	XP_005259970.1:p.Ala923Asp
XM_024451518.1:c.1664C>A	XP_024307286.1:p.Ala555Asp
NM_000528.4:c.2765C>A MANE Select	NP_000519.2:p.Ala922Asp
NM_001173498.2:c.2762C>A	NP_001166969.1:p.Ala921Asp