Canonical Allele Identifier: CA9225941
Gene: MAN2B1 HGNC NCBI

Linked Data

dbSNP Id: rs774352491

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12647561T>C , CM000681.2:g.12647561T>C GRCh38
NC_000019.9:g.12758375T>C , CM000681.1:g.12758375T>C GRCh37
NC_000019.8:g.12619375T>C NCBI36
NG_008318.1:g.24217A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000456935.7:c.2702A>G MANE Select ENSP00000395473.2:p.His901Arg
ENST00000221363.8:c.2699A>G ENSP00000221363.4:p.His900Arg
ENST00000456935.6:c.2702A>G ENSP00000395473.2:p.His901Arg
ENST00000466794.5:n.3292A>G
ENST00000469423.1:n.24A>G
ENST00000493218.5:n.113A>G
ENST00000597692.1:c.261A>G
NM_000528.3:c.2702A>G NP_000519.2:p.His901Arg
NM_001173498.1:c.2699A>G NP_001166969.1:p.His900Arg
XM_005259913.1:c.2705A>G XP_005259970.1:p.His902Arg
XM_011528017.1:c.1601A>G XP_011526319.1:p.His534Arg
XM_005259913.2:c.2705A>G XP_005259970.1:p.His902Arg
XM_024451518.1:c.1601A>G XP_024307286.1:p.His534Arg
NM_000528.4:c.2702A>G MANE Select NP_000519.2:p.His901Arg
NM_001173498.2:c.2699A>G NP_001166969.1:p.His900Arg