Canonical Allele Identifier: CA666361091
Gene: MBL2 HGNC NCBI

Linked Data

dbSNP Id: rs1189061022

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52771927T>C , CM000672.2:g.52771927T>C GRCh38
NC_000010.10:g.54531687T>C , CM000672.1:g.54531687T>C GRCh37
NC_000010.9:g.54201693T>C NCBI36
NG_008196.1:g.4774A>G , LRG_154:g.4774A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000674931.1:c.-9-283A>G MANE Select ENSP00000502789.1:n.-9-283A>G
ENST00000675947.1:c.-24-268A>G ENSP00000502615.1:n.-24-268A>G
XM_006717861.2:c.-24-268A>G XP_006717924.1:n.-24-268A>G
XM_011539816.1:c.-9-283A>G XP_011538118.1:n.-9-283A>G
XM_006717861.4:c.-24-268A>G XP_006717924.1:n.-24-268A>G
XM_011539816.3:c.-9-283A>G XP_011538118.1:n.-9-283A>G
NM_001378373.1:c.-9-283A>G MANE Select NP_001365302.1:n.-9-283A>G
NM_001378374.1:c.-24-268A>G NP_001365303.1:n.-24-268A>G