Canonical Allele Identifier: CA2323500080
Gene: MAN2B1 HGNC NCBI

Linked Data

dbSNP Id: rs2023806568
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12650109_12650123del , CM000681.2:g.12650109_12650123del GRCh38
NC_000019.9:g.12760923_12760937del , CM000681.1:g.12760923_12760937del GRCh37
NC_000019.8:g.12621923_12621937del NCBI36
NG_008318.1:g.21661_21675del

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.2152_2165+1del
ENST00000221363.8:c.2149_2162+1del
ENST00000456935.6:c.2152_2165+1del
ENST00000466794.5:n.2742_2755+1del
NM_000528.3:c.2152_2165+1del
NM_001173498.1:c.2149_2162+1del
XM_005259913.1:c.2155_2168+1del
XM_011528017.1:c.1051_1064+1del
XM_005259913.2:c.2155_2168+1del
XM_024451518.1:c.1051_1064+1del
NM_000528.4:c.2152_2165+1del
NM_001173498.2:c.2149_2162+1del
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