Canonical Allele Identifier: CA1910259478
Gene: MBL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52771796C= , CM000672.2:g.52771796C= GRCh38
NC_000010.10:g.54531556C= , CM000672.1:g.54531556C= GRCh37
NC_000010.9:g.54201562C= NCBI36
NG_008196.1:g.4905G= , LRG_154:g.4905G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000674931.1:c.-9-152G= MANE Select ENSP00000502789.1:n.-9-152G=
ENST00000675947.1:c.-24-137G= ENSP00000502615.1:n.-24-137G=
XM_006717861.2:c.-24-137G= XP_006717924.1:n.-24-137G=
XM_011539816.1:c.-9-152G= XP_011538118.1:n.-9-152G=
XM_006717861.4:c.-24-137G= XP_006717924.1:n.-24-137G=
XM_011539816.3:c.-9-152G= XP_011538118.1:n.-9-152G=
NM_001378373.1:c.-9-152G= MANE Select NP_001365302.1:n.-9-152G=
NM_001378374.1:c.-24-137G= NP_001365303.1:n.-24-137G=