Canonical Allele Identifier: CA653288479
Gene: MBL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52771749A>G , CM000672.2:g.52771749A>G GRCh38
NC_000010.10:g.54531509A>G , CM000672.1:g.54531509A>G GRCh37
NC_000010.9:g.54201515A>G NCBI36
NG_008196.1:g.4952T>C , LRG_154:g.4952T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000674931.1:c.-9-105T>C MANE Select ENSP00000502789.1:n.-9-105T>C
ENST00000675947.1:c.-24-90T>C ENSP00000502615.1:n.-24-90T>C
XM_006717861.2:c.-24-90T>C XP_006717924.1:n.-24-90T>C
XM_011539816.1:c.-9-105T>C XP_011538118.1:n.-9-105T>C
XM_006717861.4:c.-24-90T>C XP_006717924.1:n.-24-90T>C
XM_011539816.3:c.-9-105T>C XP_011538118.1:n.-9-105T>C
NM_001378373.1:c.-9-105T>C MANE Select NP_001365302.1:n.-9-105T>C
NM_001378374.1:c.-24-90T>C NP_001365303.1:n.-24-90T>C