Canonical Allele Identifier: CA505624940

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12767796G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12656982G>A , CM000681.2:g.12656982G>A	GRCh38
NC_000019.9:g.12767796G>A , CM000681.1:g.12767796G>A	GRCh37
NC_000019.8:g.12628796G>A	NCBI36
NG_008318.1:g.14796C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1494C>T MANE Select	ENSP00000395473.2:p.Ile498=
ENST00000221363.8:c.1491C>T	ENSP00000221363.4:p.Ile497=
ENST00000433513.5:n.100C>T
ENST00000456935.6:c.1494C>T	ENSP00000395473.2:p.Ile498=
ENST00000466794.5:n.1393C>T
ENST00000495617.1:n.670C>T
ENST00000593686.1:c.104C>T
ENST00000595880.5:n.91C>T
NM_000528.3:c.1494C>T	NP_000519.2:p.Ile498=
NM_001173498.1:c.1491C>T	NP_001166969.1:p.Ile497=
XM_005259913.1:c.1497C>T	XP_005259970.1:p.Ile499=
XM_011528017.1:c.393C>T	XP_011526319.1:p.Ile131=
XM_005259913.2:c.1497C>T	XP_005259970.1:p.Ile499=
XM_024451518.1:c.393C>T	XP_024307286.1:p.Ile131=
NM_000528.4:c.1494C>T MANE Select	NP_000519.2:p.Ile498=
NM_001173498.2:c.1491C>T	NP_001166969.1:p.Ile497=