Canonical Allele Identifier: CA376540251

Gene: MBL2

Linked Data

• COSMIC: COSM4700991
• MyVariant Identifiers: chr10:g.54531352A>G (hg19) ; chr10:g.52771592A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.52771592A>G , CM000672.2:g.52771592A>G	GRCh38
NC_000010.10:g.54531352A>G , CM000672.1:g.54531352A>G	GRCh37
NC_000010.9:g.54201358A>G	NCBI36
NG_008196.1:g.5109T>C , LRG_154:g.5109T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674931.1:c.44T>C MANE Select	ENSP00000502789.1:p.Val15Ala
ENST00000675947.1:c.44T>C	ENSP00000502615.1:p.Val15Ala
ENST00000373968.3:c.44T>C	ENSP00000363079.3:p.Val15Ala
NM_000242.2:c.44T>C , LRG_154t1:c.44T>C	NP_000233.1:p.Val15Ala
XM_006717861.2:c.44T>C	XP_006717924.1:p.Val15Ala
XM_011539816.1:c.44T>C	XP_011538118.1:p.Val15Ala
XM_006717861.4:c.44T>C	XP_006717924.1:p.Val15Ala
XM_011539816.3:c.44T>C	XP_011538118.1:p.Val15Ala
NM_000242.3:c.44T>C	NP_000233.1:p.Val15Ala
NM_001378373.1:c.44T>C MANE Select	NP_001365302.1:p.Val15Ala
NM_001378374.1:c.44T>C	NP_001365303.1:p.Val15Ala