Canonical Allele Identifier: CA404252549

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12774525A>T (hg19) ; chr19:g.12663711A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12663711A>T , CM000681.2:g.12663711A>T	GRCh38
NC_000019.9:g.12774525A>T , CM000681.1:g.12774525A>T	GRCh37
NC_000019.8:g.12635525A>T	NCBI36
NG_008318.1:g.8067T>A
NG_015814.1:g.1908A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.755T>A MANE Select	ENSP00000395473.2:p.Leu252His
ENST00000221363.8:c.755T>A	ENSP00000221363.4:p.Leu252His
ENST00000456935.6:c.755T>A	ENSP00000395473.2:p.Leu252His
ENST00000466794.5:n.737T>A
ENST00000486847.2:c.458T>A	ENSP00000470174.1:p.Leu153His
NM_000528.3:c.755T>A	NP_000519.2:p.Leu252His
NM_001173498.1:c.755T>A	NP_001166969.1:p.Leu252His
XM_005259913.1:c.755T>A	XP_005259970.1:p.Leu252His
XM_005259913.2:c.755T>A	XP_005259970.1:p.Leu252His
XM_024451518.1:c.-264T>A	XP_024307286.1:n.-264T>A
NM_000528.4:c.755T>A MANE Select	NP_000519.2:p.Leu252His
NM_001173498.2:c.755T>A	NP_001166969.1:p.Leu252His