Canonical Allele Identifier: CA433834471

Gene: LAMB2

Linked Data

• ClinVar Variation Id: 2946364
• ClinVar RCV Id: RCV003806650
• MyVariant Identifiers: chr3:g.49162865A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125432A>G , CM000665.2:g.49125432A>G	GRCh38
NC_000003.11:g.49162865A>G , CM000665.1:g.49162865A>G	GRCh37
NC_000003.10:g.49137869A>G	NCBI36
NG_008094.1:g.12735T>C
NG_054716.1:g.507T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2541T>C MANE Select	ENSP00000307156.4:p.Ser847=
ENST00000305544.8:c.2541T>C	ENSP00000307156.4:p.Ser847=
ENST00000418109.5:c.2541T>C	ENSP00000388325.1:p.Ser847=
ENST00000464891.5:n.290T>C
ENST00000477701.1:n.414T>C
ENST00000483057.1:n.141T>C
ENST00000486298.5:n.426-263T>C
NM_002292.3:c.2541T>C	NP_002283.3:p.Ser847=
XM_005265127.3:c.2541T>C	XP_005265184.1:p.Ser847=
XM_005265127.4:c.2541T>C	XP_005265184.1:p.Ser847=
NM_002292.4:c.2541T>C MANE Select	NP_002283.3:p.Ser847=