Canonical Allele Identifier: CA404258733

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12776612G>T (hg19) ; chr19:g.12665798G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665798G>T , CM000681.2:g.12665798G>T	GRCh38
NC_000019.9:g.12776612G>T , CM000681.1:g.12776612G>T	GRCh37
NC_000019.8:g.12637612G>T	NCBI36
NG_008318.1:g.5980C>A
NG_015814.1:g.3995G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.167C>A MANE Select	ENSP00000395473.2:p.Pro56His
ENST00000221363.8:c.167C>A	ENSP00000221363.4:p.Pro56His
ENST00000456935.6:c.167C>A	ENSP00000395473.2:p.Pro56His
ENST00000466794.5:n.149C>A
ENST00000486847.2:c.160-273C>A	ENSP00000470174.1:n.160-273C>A
ENST00000596512.5:n.201-273C>A
ENST00000597961.1:c.158C>A	ENSP00000472710.1:p.Pro53His
ENST00000598876.1:c.194C>A	ENSP00000470533.1:p.Pro65His
ENST00000600281.1:n.208C>A
NM_000528.3:c.167C>A	NP_000519.2:p.Pro56His
NM_001173498.1:c.167C>A	NP_001166969.1:p.Pro56His
XM_005259913.1:c.167C>A	XP_005259970.1:p.Pro56His
XM_005259913.2:c.167C>A	XP_005259970.1:p.Pro56His
XM_024451518.1:c.-852C>A	XP_024307286.1:n.-852C>A
NM_000528.4:c.167C>A MANE Select	NP_000519.2:p.Pro56His
NM_001173498.2:c.167C>A	NP_001166969.1:p.Pro56His