Canonical Allele Identifier: CA505625064

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12769301A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12658487A>G , CM000681.2:g.12658487A>G	GRCh38
NC_000019.9:g.12769301A>G , CM000681.1:g.12769301A>G	GRCh37
NC_000019.8:g.12630301A>G	NCBI36
NG_008318.1:g.13291T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1050T>C MANE Select	ENSP00000395473.2:p.His350=
ENST00000221363.8:c.1047T>C	ENSP00000221363.4:p.His349=
ENST00000456935.6:c.1050T>C	ENSP00000395473.2:p.His350=
ENST00000465830.1:n.131T>C
ENST00000466794.5:n.1009-143T>C
ENST00000495617.1:n.280+244T>C
NM_000528.3:c.1050T>C	NP_000519.2:p.His350=
NM_001173498.1:c.1047T>C	NP_001166969.1:p.His349=
XM_005259913.1:c.1053T>C	XP_005259970.1:p.His351=
XM_011528017.1:c.9-143T>C	XP_011526319.1:n.9-143T>C
XM_005259913.2:c.1053T>C	XP_005259970.1:p.His351=
XM_024451518.1:c.9-143T>C	XP_024307286.1:n.9-143T>C
NM_000528.4:c.1050T>C MANE Select	NP_000519.2:p.His350=
NM_001173498.2:c.1047T>C	NP_001166969.1:p.His349=