Canonical Allele Identifier: CA404256951

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12776276A>T (hg19) ; chr19:g.12665462A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665462A>T , CM000681.2:g.12665462A>T	GRCh38
NC_000019.9:g.12776276A>T , CM000681.1:g.12776276A>T	GRCh37
NC_000019.8:g.12637276A>T	NCBI36
NG_008318.1:g.6316T>A
NG_015814.1:g.3659A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.326T>A MANE Select	ENSP00000395473.2:p.Leu109Gln
ENST00000221363.8:c.326T>A	ENSP00000221363.4:p.Leu109Gln
ENST00000456935.6:c.326T>A	ENSP00000395473.2:p.Leu109Gln
ENST00000466794.5:n.308T>A
ENST00000486847.2:c.223T>A	ENSP00000470174.1:p.Trp75Arg
ENST00000596512.5:n.264T>A
ENST00000597961.1:c.317T>A	ENSP00000472710.1:p.Leu106Gln
ENST00000598876.1:c.353T>A	ENSP00000470533.1:p.Leu118Gln
ENST00000600281.1:n.367T>A
NM_000528.3:c.326T>A	NP_000519.2:p.Leu109Gln
NM_001173498.1:c.326T>A	NP_001166969.1:p.Leu109Gln
XM_005259913.1:c.326T>A	XP_005259970.1:p.Leu109Gln
XM_005259913.2:c.326T>A	XP_005259970.1:p.Leu109Gln
XM_024451518.1:c.-693T>A	XP_024307286.1:n.-693T>A
NM_000528.4:c.326T>A MANE Select	NP_000519.2:p.Leu109Gln
NM_001173498.2:c.326T>A	NP_001166969.1:p.Leu109Gln