Canonical Allele Identifier: CA505770991

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12760968T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12650154T>A , CM000681.2:g.12650154T>A	GRCh38
NC_000019.9:g.12760968T>A , CM000681.1:g.12760968T>A	GRCh37
NC_000019.8:g.12621968T>A	NCBI36
NG_008318.1:g.21624A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2115A>T MANE Select	ENSP00000395473.2:p.Pro705=
ENST00000221363.8:c.2112A>T	ENSP00000221363.4:p.Pro704=
ENST00000456935.6:c.2115A>T	ENSP00000395473.2:p.Pro705=
ENST00000466794.5:n.2705A>T
NM_000528.3:c.2115A>T	NP_000519.2:p.Pro705=
NM_001173498.1:c.2112A>T	NP_001166969.1:p.Pro704=
XM_005259913.1:c.2118A>T	XP_005259970.1:p.Pro706=
XM_011528017.1:c.1014A>T	XP_011526319.1:p.Pro338=
XM_005259913.2:c.2118A>T	XP_005259970.1:p.Pro706=
XM_024451518.1:c.1014A>T	XP_024307286.1:p.Pro338=
NM_000528.4:c.2115A>T MANE Select	NP_000519.2:p.Pro705=
NM_001173498.2:c.2112A>T	NP_001166969.1:p.Pro704=