Canonical Allele Identifier: CA505624969

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12767847C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12657033C>A , CM000681.2:g.12657033C>A	GRCh38
NC_000019.9:g.12767847C>A , CM000681.1:g.12767847C>A	GRCh37
NC_000019.8:g.12628847C>A	NCBI36
NG_008318.1:g.14745G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1443G>T MANE Select	ENSP00000395473.2:p.Ala481=
ENST00000221363.8:c.1440G>T	ENSP00000221363.4:p.Ala480=
ENST00000433513.5:n.49G>T
ENST00000456935.6:c.1443G>T	ENSP00000395473.2:p.Ala481=
ENST00000466794.5:n.1342G>T
ENST00000495617.1:n.619G>T
ENST00000593686.1:c.53G>T
ENST00000595880.5:n.40G>T
NM_000528.3:c.1443G>T	NP_000519.2:p.Ala481=
NM_001173498.1:c.1440G>T	NP_001166969.1:p.Ala480=
XM_005259913.1:c.1446G>T	XP_005259970.1:p.Ala482=
XM_011528017.1:c.342G>T	XP_011526319.1:p.Ala114=
XM_005259913.2:c.1446G>T	XP_005259970.1:p.Ala482=
XM_024451518.1:c.342G>T	XP_024307286.1:p.Ala114=
NM_000528.4:c.1443G>T MANE Select	NP_000519.2:p.Ala481=
NM_001173498.2:c.1440G>T	NP_001166969.1:p.Ala480=