Canonical Allele Identifier: CA404256999

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12776280A>T (hg19) ; chr19:g.12665466A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665466A>T , CM000681.2:g.12665466A>T	GRCh38
NC_000019.9:g.12776280A>T , CM000681.1:g.12776280A>T	GRCh37
NC_000019.8:g.12637280A>T	NCBI36
NG_008318.1:g.6312T>A
NG_015814.1:g.3663A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.322T>A MANE Select	ENSP00000395473.2:p.Leu108Met
ENST00000221363.8:c.322T>A	ENSP00000221363.4:p.Leu108Met
ENST00000456935.6:c.322T>A	ENSP00000395473.2:p.Leu108Met
ENST00000466794.5:n.304T>A
ENST00000486847.2:c.219T>A	ENSP00000470174.1:p.Pro73=
ENST00000596512.5:n.260T>A
ENST00000597961.1:c.313T>A	ENSP00000472710.1:p.Leu105Met
ENST00000598876.1:c.349T>A	ENSP00000470533.1:p.Leu117Met
ENST00000600281.1:n.363T>A
NM_000528.3:c.322T>A	NP_000519.2:p.Leu108Met
NM_001173498.1:c.322T>A	NP_001166969.1:p.Leu108Met
XM_005259913.1:c.322T>A	XP_005259970.1:p.Leu108Met
XM_005259913.2:c.322T>A	XP_005259970.1:p.Leu108Met
XM_024451518.1:c.-697T>A	XP_024307286.1:n.-697T>A
NM_000528.4:c.322T>A MANE Select	NP_000519.2:p.Leu108Met
NM_001173498.2:c.322T>A	NP_001166969.1:p.Leu108Met