Canonical Allele Identifier: CA404247794
Gene: MAN2B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12658235T>G , CM000681.2:g.12658235T>G GRCh38
NC_000019.9:g.12769049T>G , CM000681.1:g.12769049T>G GRCh37
NC_000019.8:g.12630049T>G NCBI36
NG_008318.1:g.13543A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000456935.7:c.1219A>C MANE Select ENSP00000395473.2:p.Asn407His
ENST00000221363.8:c.1216A>C ENSP00000221363.4:p.Asn406His
ENST00000456935.6:c.1219A>C ENSP00000395473.2:p.Asn407His
ENST00000465830.1:n.383A>C
ENST00000466794.5:n.1118A>C
ENST00000495617.1:n.281-475A>C
NM_000528.3:c.1219A>C NP_000519.2:p.Asn407His
NM_001173498.1:c.1216A>C NP_001166969.1:p.Asn406His
XM_005259913.1:c.1222A>C XP_005259970.1:p.Asn408His
XM_011528017.1:c.118A>C XP_011526319.1:p.Asn40His
XM_005259913.2:c.1222A>C XP_005259970.1:p.Asn408His
XM_024451518.1:c.118A>C XP_024307286.1:p.Asn40His
NM_000528.4:c.1219A>C MANE Select NP_000519.2:p.Asn407His
NM_001173498.2:c.1216A>C NP_001166969.1:p.Asn406His