Canonical Allele Identifier: CA2609210124
Gene: MBL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52771327dup , CM000672.2:g.52771327dup GRCh38
NC_000010.10:g.54531087dup , CM000672.1:g.54531087dup GRCh37
NC_000010.9:g.54201093dup NCBI36
NG_008196.1:g.5374dup , LRG_154:g.5374dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000674931.1:c.187+122dup MANE Select ENSP00000502789.1:n.187+122dup
ENST00000675947.1:c.187+122dup ENSP00000502615.1:n.187+122dup
ENST00000373968.3:c.187+122dup ENSP00000363079.3:n.187+122dup
NM_000242.2:c.187+122dup , LRG_154t1:c.187+122dup NP_000233.1:n.187+122dup
XM_006717861.2:c.187+122dup XP_006717924.1:n.187+122dup
XM_011539816.1:c.187+122dup XP_011538118.1:n.187+122dup
XM_006717861.4:c.187+122dup XP_006717924.1:n.187+122dup
XM_011539816.3:c.187+122dup XP_011538118.1:n.187+122dup
NM_000242.3:c.187+122dup NP_000233.1:n.187+122dup
NM_001378373.1:c.187+122dup MANE Select NP_001365302.1:n.187+122dup
NM_001378374.1:c.187+122dup NP_001365303.1:n.187+122dup