Canonical Allele Identifier: CA505624999

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12768275G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12657461G>C , CM000681.2:g.12657461G>C	GRCh38
NC_000019.9:g.12768275G>C , CM000681.1:g.12768275G>C	GRCh37
NC_000019.8:g.12629275G>C	NCBI36
NG_008318.1:g.14317C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1404C>G MANE Select	ENSP00000395473.2:p.Gly468=
ENST00000221363.8:c.1401C>G	ENSP00000221363.4:p.Gly467=
ENST00000456935.6:c.1404C>G	ENSP00000395473.2:p.Gly468=
ENST00000465830.1:n.568C>G
ENST00000466794.5:n.1303C>G
ENST00000495617.1:n.580C>G
ENST00000593686.1:c.14C>G
NM_000528.3:c.1404C>G	NP_000519.2:p.Gly468=
NM_001173498.1:c.1401C>G	NP_001166969.1:p.Gly467=
XM_005259913.1:c.1407C>G	XP_005259970.1:p.Gly469=
XM_011528017.1:c.303C>G	XP_011526319.1:p.Gly101=
XM_005259913.2:c.1407C>G	XP_005259970.1:p.Gly469=
XM_024451518.1:c.303C>G	XP_024307286.1:p.Gly101=
NM_000528.4:c.1404C>G MANE Select	NP_000519.2:p.Gly468=
NM_001173498.2:c.1401C>G	NP_001166969.1:p.Gly467=