Canonical Allele Identifier: CA1910259550
Gene: MBL2 HGNC NCBI

Linked Data

dbSNP Id: rs1840399717

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52771935del , CM000672.2:g.52771935del GRCh38
NC_000010.10:g.54531695del , CM000672.1:g.54531695del GRCh37
NC_000010.9:g.54201701del NCBI36
NG_008196.1:g.4766del , LRG_154:g.4766del

Transcript Alleles

HGVS Amino-acid change
ENST00000674931.1:c.-9-291del MANE Select ENSP00000502789.1:n.-9-291del
ENST00000675947.1:c.-24-276del ENSP00000502615.1:n.-24-276del
XM_006717861.2:c.-24-276del XP_006717924.1:n.-24-276del
XM_011539816.1:c.-9-291del XP_011538118.1:n.-9-291del
XM_006717861.4:c.-24-276del XP_006717924.1:n.-24-276del
XM_011539816.3:c.-9-291del XP_011538118.1:n.-9-291del
NM_001378373.1:c.-9-291del MANE Select NP_001365302.1:n.-9-291del
NM_001378374.1:c.-24-276del NP_001365303.1:n.-24-276del