Canonical Allele Identifier: CA1910259576
Gene: MBL2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52771994A= , CM000672.2:g.52771994A= GRCh38
NC_000010.10:g.54531754A= , CM000672.1:g.54531754A= GRCh37
NC_000010.9:g.54201760A= NCBI36
NG_008196.1:g.4707T= , LRG_154:g.4707T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000674931.1:c.-9-350T= MANE Select ENSP00000502789.1:n.-9-350T=
ENST00000675947.1:c.-24-335T= ENSP00000502615.1:n.-24-335T=
XM_006717861.2:c.-24-335T= XP_006717924.1:n.-24-335T=
XM_011539816.1:c.-9-350T= XP_011538118.1:n.-9-350T=
XM_006717861.4:c.-24-335T= XP_006717924.1:n.-24-335T=
XM_011539816.3:c.-9-350T= XP_011538118.1:n.-9-350T=
NM_001378373.1:c.-9-350T= MANE Select NP_001365302.1:n.-9-350T=
NM_001378374.1:c.-24-335T= NP_001365303.1:n.-24-335T=
Search 100 bp 5'
Search 100 bp 3'