Canonical Allele Identifier: CA404237897

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12758322G>T (hg19) ; chr19:g.12647508G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647508G>T , CM000681.2:g.12647508G>T	GRCh38
NC_000019.9:g.12758322G>T , CM000681.1:g.12758322G>T	GRCh37
NC_000019.8:g.12619322G>T	NCBI36
NG_008318.1:g.24270C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2755C>A MANE Select	ENSP00000395473.2:p.His919Asn
ENST00000221363.8:c.2752C>A	ENSP00000221363.4:p.His918Asn
ENST00000456935.6:c.2755C>A	ENSP00000395473.2:p.His919Asn
ENST00000466794.5:n.3345C>A
ENST00000469423.1:n.77C>A
ENST00000493218.5:n.166C>A
ENST00000597692.1:c.314C>A
NM_000528.3:c.2755C>A	NP_000519.2:p.His919Asn
NM_001173498.1:c.2752C>A	NP_001166969.1:p.His918Asn
XM_005259913.1:c.2758C>A	XP_005259970.1:p.His920Asn
XM_011528017.1:c.1654C>A	XP_011526319.1:p.His552Asn
XM_005259913.2:c.2758C>A	XP_005259970.1:p.His920Asn
XM_024451518.1:c.1654C>A	XP_024307286.1:p.His552Asn
NM_000528.4:c.2755C>A MANE Select	NP_000519.2:p.His919Asn
NM_001173498.2:c.2752C>A	NP_001166969.1:p.His918Asn