Canonical Allele Identifier: CA505626789

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12776608T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665794T>G , CM000681.2:g.12665794T>G	GRCh38
NC_000019.9:g.12776608T>G , CM000681.1:g.12776608T>G	GRCh37
NC_000019.8:g.12637608T>G	NCBI36
NG_008318.1:g.5984A>C
NG_015814.1:g.3991T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.171A>C MANE Select	ENSP00000395473.2:p.Thr57=
ENST00000221363.8:c.171A>C	ENSP00000221363.4:p.Thr57=
ENST00000456935.6:c.171A>C	ENSP00000395473.2:p.Thr57=
ENST00000466794.5:n.153A>C
ENST00000486847.2:c.160-269A>C	ENSP00000470174.1:n.160-269A>C
ENST00000596512.5:n.201-269A>C
ENST00000597961.1:c.162A>C	ENSP00000472710.1:p.Thr54=
ENST00000598876.1:c.198A>C	ENSP00000470533.1:p.Thr66=
ENST00000600281.1:n.212A>C
NM_000528.3:c.171A>C	NP_000519.2:p.Thr57=
NM_001173498.1:c.171A>C	NP_001166969.1:p.Thr57=
XM_005259913.1:c.171A>C	XP_005259970.1:p.Thr57=
XM_005259913.2:c.171A>C	XP_005259970.1:p.Thr57=
XM_024451518.1:c.-848A>C	XP_024307286.1:n.-848A>C
NM_000528.4:c.171A>C MANE Select	NP_000519.2:p.Thr57=
NM_001173498.2:c.171A>C	NP_001166969.1:p.Thr57=