Canonical Allele Identifier: CA505624695

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12766553G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12655739G>T , CM000681.2:g.12655739G>T	GRCh38
NC_000019.9:g.12766553G>T , CM000681.1:g.12766553G>T	GRCh37
NC_000019.8:g.12627553G>T	NCBI36
NG_008318.1:g.16039C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.1785C>A MANE Select	ENSP00000395473.2:p.Pro595=
ENST00000221363.8:c.1782C>A	ENSP00000221363.4:p.Pro594=
ENST00000433513.5:n.391C>A
ENST00000456935.6:c.1785C>A	ENSP00000395473.2:p.Pro595=
ENST00000466794.5:n.2375C>A
ENST00000593686.1:c.378C>A
ENST00000595880.5:n.382C>A
ENST00000596591.1:c.149C>A
NM_000528.3:c.1785C>A	NP_000519.2:p.Pro595=
NM_001173498.1:c.1782C>A	NP_001166969.1:p.Pro594=
XM_005259913.1:c.1788C>A	XP_005259970.1:p.Pro596=
XM_011528017.1:c.684C>A	XP_011526319.1:p.Pro228=
XM_005259913.2:c.1788C>A	XP_005259970.1:p.Pro596=
XM_024451518.1:c.684C>A	XP_024307286.1:p.Pro228=
NM_000528.4:c.1785C>A MANE Select	NP_000519.2:p.Pro595=
NM_001173498.2:c.1782C>A	NP_001166969.1:p.Pro594=