Canonical Allele Identifier: CA404245060

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12655860G>C , CM000681.2:g.12655860G>C	GRCh38
NC_000019.9:g.12766674G>C , CM000681.1:g.12766674G>C	GRCh37
NC_000019.8:g.12627674G>C	NCBI36
NG_008318.1:g.15918C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000528.4:c.1664C>G MANE Select	NP_000519.2:p.Ser555Ter
ENST00000456935.7:c.1664C>G MANE Select	ENSP00000395473.2:p.Ser555Ter
NM_000528.3:c.1664C>G	NP_000519.2:p.Ser555Ter
NM_001173498.1:c.1661C>G	NP_001166969.1:p.Ser554Ter
NM_001173498.2:c.1661C>G	NP_001166969.1:p.Ser554Ter
ENST00000221363.8:c.1661C>G	ENSP00000221363.4:p.Ser554Ter
ENST00000433513.5:n.270C>G
ENST00000456935.6:c.1664C>G	ENSP00000395473.2:p.Ser555Ter
ENST00000466794.5:n.2254C>G
ENST00000593686.1:c.257C>G
ENST00000595880.5:n.261C>G
ENST00000596591.1:c.28C>G
XM_005259913.1:c.1667C>G	XP_005259970.1:p.Ser556Ter
XM_005259913.2:c.1667C>G	XP_005259970.1:p.Ser556Ter
XM_011528017.1:c.563C>G	XP_011526319.1:p.Ser188Ter
XM_024451518.1:c.563C>G	XP_024307286.1:p.Ser188Ter