Canonical Allele Identifier: CA666356484

Gene: MBL2

Linked Data

• dbSNP Id: rs1278969832
• gnomAD v3: 10-52766221-GA-G
• gnomAD v4: 10-52766221-GA-G
• MyVariant Identifiers: chr10:g.54525982del (hg19) ; chr10:g.52766222del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.52766223del , CM000672.2:g.52766223del	GRCh38
NC_000010.10:g.54525983del , CM000672.1:g.54525983del	GRCh37
NC_000010.9:g.54195989del	NCBI36
NG_008196.1:g.10479del , LRG_154:g.10479del

Transcript Alleles

HGVS	Amino-acid change
ENST00000674931.1:c.*1915del MANE Select	ENSP00000502789.1:n.*1915del
ENST00000675947.1:c.*1915del	ENSP00000502615.1:n.*1915del
ENST00000373968.3:c.*1915del	ENSP00000363079.3:n.*1915del
NM_000242.2:c.*1915del , LRG_154t1:c.*1915del	NP_000233.1:n.*1915del
XM_006717861.2:c.*1915del	XP_006717924.1:n.*1915del
XM_011539816.1:c.*1915del	XP_011538118.1:n.*1915del
XM_006717861.4:c.*1915del	XP_006717924.1:n.*1915del
XM_011539816.3:c.*1915del	XP_011538118.1:n.*1915del
NM_000242.3:c.*1915del	NP_000233.1:n.*1915del
NM_001378373.1:c.*1915del MANE Select	NP_001365302.1:n.*1915del
NM_001378374.1:c.*1915del	NP_001365303.1:n.*1915del