Canonical Allele Identifier: CA505770826

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12758401C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647587C>A , CM000681.2:g.12647587C>A	GRCh38
NC_000019.9:g.12758401C>A , CM000681.1:g.12758401C>A	GRCh37
NC_000019.8:g.12619401C>A	NCBI36
NG_008318.1:g.24191G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2676G>T MANE Select	ENSP00000395473.2:p.Leu892=
ENST00000221363.8:c.2673G>T	ENSP00000221363.4:p.Leu891=
ENST00000456935.6:c.2676G>T	ENSP00000395473.2:p.Leu892=
ENST00000466794.5:n.3266G>T
ENST00000493218.5:n.87G>T
ENST00000597692.1:c.235G>T
NM_000528.3:c.2676G>T	NP_000519.2:p.Leu892=
NM_001173498.1:c.2673G>T	NP_001166969.1:p.Leu891=
XM_005259913.1:c.2679G>T	XP_005259970.1:p.Leu893=
XM_011528017.1:c.1575G>T	XP_011526319.1:p.Leu525=
XM_005259913.2:c.2679G>T	XP_005259970.1:p.Leu893=
XM_024451518.1:c.1575G>T	XP_024307286.1:p.Leu525=
NM_000528.4:c.2676G>T MANE Select	NP_000519.2:p.Leu892=
NM_001173498.2:c.2673G>T	NP_001166969.1:p.Leu891=