Canonical Allele Identifier: CA13220763
Gene: MBL2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs7096206

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52771925G>C , CM000672.2:g.52771925G>C GRCh38
NC_000010.10:g.54531685G>C , CM000672.1:g.54531685G>C GRCh37
NC_000010.9:g.54201691G>C NCBI36
NG_008196.1:g.4776C>G , LRG_154:g.4776C>G

Transcript Alleles

HGVS Amino-acid change
XM_006717861.2:c.-24-266C>G XP_006717924.1:p.=
XM_011539816.1:c.-9-281C>G XP_011538118.1:p.=
XM_006717861.4:c.-24-266C>G XP_006717924.1:p.=
XM_011539816.3:c.-9-281C>G XP_011538118.1:p.=