Canonical Allele Identifier: CA404257197

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12776297T>A (hg19) ; chr19:g.12665483T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665483T>A , CM000681.2:g.12665483T>A	GRCh38
NC_000019.9:g.12776297T>A , CM000681.1:g.12776297T>A	GRCh37
NC_000019.8:g.12637297T>A	NCBI36
NG_008318.1:g.6295A>T
NG_015814.1:g.3680T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.305A>T MANE Select	ENSP00000395473.2:p.Asp102Val
ENST00000221363.8:c.305A>T	ENSP00000221363.4:p.Asp102Val
ENST00000456935.6:c.305A>T	ENSP00000395473.2:p.Asp102Val
ENST00000466794.5:n.287A>T
ENST00000486847.2:c.202A>T	ENSP00000470174.1:p.Thr68Ser
ENST00000596512.5:n.243A>T
ENST00000597961.1:c.296A>T	ENSP00000472710.1:p.Asp99Val
ENST00000598876.1:c.332A>T	ENSP00000470533.1:p.Asp111Val
ENST00000600281.1:n.346A>T
NM_000528.3:c.305A>T	NP_000519.2:p.Asp102Val
NM_001173498.1:c.305A>T	NP_001166969.1:p.Asp102Val
XM_005259913.1:c.305A>T	XP_005259970.1:p.Asp102Val
XM_005259913.2:c.305A>T	XP_005259970.1:p.Asp102Val
XM_024451518.1:c.-714A>T	XP_024307286.1:n.-714A>T
NM_000528.4:c.305A>T MANE Select	NP_000519.2:p.Asp102Val
NM_001173498.2:c.305A>T	NP_001166969.1:p.Asp102Val