Canonical Allele Identifier: CA404252532

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12774522A>T (hg19) ; chr19:g.12663708A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12663708A>T , CM000681.2:g.12663708A>T	GRCh38
NC_000019.9:g.12774522A>T , CM000681.1:g.12774522A>T	GRCh37
NC_000019.8:g.12635522A>T	NCBI36
NG_008318.1:g.8070T>A
NG_015814.1:g.1905A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.758T>A MANE Select	ENSP00000395473.2:p.Phe253Tyr
ENST00000221363.8:c.758T>A	ENSP00000221363.4:p.Phe253Tyr
ENST00000456935.6:c.758T>A	ENSP00000395473.2:p.Phe253Tyr
ENST00000466794.5:n.740T>A
ENST00000486847.2:c.461T>A	ENSP00000470174.1:p.Phe154Tyr
NM_000528.3:c.758T>A	NP_000519.2:p.Phe253Tyr
NM_001173498.1:c.758T>A	NP_001166969.1:p.Phe253Tyr
XM_005259913.1:c.758T>A	XP_005259970.1:p.Phe253Tyr
XM_005259913.2:c.758T>A	XP_005259970.1:p.Phe253Tyr
XM_024451518.1:c.-261T>A	XP_024307286.1:n.-261T>A
NM_000528.4:c.758T>A MANE Select	NP_000519.2:p.Phe253Tyr
NM_001173498.2:c.758T>A	NP_001166969.1:p.Phe253Tyr