Canonical Allele Identifier: CA505626681

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12776572A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665758A>C , CM000681.2:g.12665758A>C	GRCh38
NC_000019.9:g.12776572A>C , CM000681.1:g.12776572A>C	GRCh37
NC_000019.8:g.12637572A>C	NCBI36
NG_008318.1:g.6020T>G
NG_015814.1:g.3955A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.207T>G MANE Select	ENSP00000395473.2:p.Pro69=
ENST00000221363.8:c.207T>G	ENSP00000221363.4:p.Pro69=
ENST00000456935.6:c.207T>G	ENSP00000395473.2:p.Pro69=
ENST00000466794.5:n.189T>G
ENST00000486847.2:c.160-233T>G	ENSP00000470174.1:n.160-233T>G
ENST00000596512.5:n.201-233T>G
ENST00000597961.1:c.198T>G	ENSP00000472710.1:p.Pro66=
ENST00000598876.1:c.234T>G	ENSP00000470533.1:p.Pro78=
ENST00000600281.1:n.248T>G
NM_000528.3:c.207T>G	NP_000519.2:p.Pro69=
NM_001173498.1:c.207T>G	NP_001166969.1:p.Pro69=
XM_005259913.1:c.207T>G	XP_005259970.1:p.Pro69=
XM_005259913.2:c.207T>G	XP_005259970.1:p.Pro69=
XM_024451518.1:c.-812T>G	XP_024307286.1:n.-812T>G
NM_000528.4:c.207T>G MANE Select	NP_000519.2:p.Pro69=
NM_001173498.2:c.207T>G	NP_001166969.1:p.Pro69=