Canonical Allele Identifier: CA1910259653
Gene: MBL2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52772131T= , CM000672.2:g.52772131T= GRCh38
NC_000010.10:g.54531891T= , CM000672.1:g.54531891T= GRCh37
NC_000010.9:g.54201897T= NCBI36
NG_008196.1:g.4570A= , LRG_154:g.4570A=

Transcript Alleles

HGVS Amino-acid change
ENST00000674931.1:c.-9-487A= MANE Select ENSP00000502789.1:n.-9-487A=
ENST00000675947.1:c.-24-472A= ENSP00000502615.1:n.-24-472A=
XM_006717861.2:c.-24-472A= XP_006717924.1:n.-24-472A=
XM_011539816.1:c.-9-487A= XP_011538118.1:n.-9-487A=
XM_006717861.4:c.-24-472A= XP_006717924.1:n.-24-472A=
XM_011539816.3:c.-9-487A= XP_011538118.1:n.-9-487A=
NM_001378373.1:c.-9-487A= MANE Select NP_001365302.1:n.-9-487A=
NM_001378374.1:c.-24-472A= NP_001365303.1:n.-24-472A=
Search 100 bp 5'
Search 100 bp 3'