Canonical Allele Identifier: CA2842057654

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12661181G>C , CM000681.2:g.12661181G>C	GRCh38
NC_000019.9:g.12771995G>C , CM000681.1:g.12771995G>C	GRCh37
NC_000019.8:g.12632995G>C	NCBI36
NG_008318.1:g.10597C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1026+79C>G MANE Select	ENSP00000395473.2:n.1026+79C>G
ENST00000221363.8:c.1026+79C>G	ENSP00000221363.4:n.1026+79C>G
ENST00000456935.6:c.1026+79C>G	ENSP00000395473.2:n.1026+79C>G
ENST00000462144.1:n.298C>G
ENST00000466794.5:n.1008+79C>G
NM_000528.3:c.1026+79C>G	NP_000519.2:n.1026+79C>G
NM_001173498.1:c.1026+79C>G	NP_001166969.1:n.1026+79C>G
XM_005259913.1:c.1026+79C>G	XP_005259970.1:n.1026+79C>G
XM_011528017.1:c.8+79C>G	XP_011526319.1:n.8+79C>G
XM_005259913.2:c.1026+79C>G	XP_005259970.1:n.1026+79C>G
XM_024451518.1:c.8+79C>G	XP_024307286.1:n.8+79C>G
NM_000528.4:c.1026+79C>G MANE Select	NP_000519.2:n.1026+79C>G
NM_001173498.2:c.1026+79C>G	NP_001166969.1:n.1026+79C>G