Canonical Allele Identifier: CA1910259569
Gene: MBL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52771979G= , CM000672.2:g.52771979G= GRCh38
NC_000010.10:g.54531739G= , CM000672.1:g.54531739G= GRCh37
NC_000010.9:g.54201745G= NCBI36
NG_008196.1:g.4722C= , LRG_154:g.4722C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000674931.1:c.-9-335C= MANE Select ENSP00000502789.1:n.-9-335C=
ENST00000675947.1:c.-24-320C= ENSP00000502615.1:n.-24-320C=
XM_006717861.2:c.-24-320C= XP_006717924.1:n.-24-320C=
XM_011539816.1:c.-9-335C= XP_011538118.1:n.-9-335C=
XM_006717861.4:c.-24-320C= XP_006717924.1:n.-24-320C=
XM_011539816.3:c.-9-335C= XP_011538118.1:n.-9-335C=
NM_001378373.1:c.-9-335C= MANE Select NP_001365302.1:n.-9-335C=
NM_001378374.1:c.-24-320C= NP_001365303.1:n.-24-320C=
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