Canonical Allele Identifier: CA352716170

Gene: LAMB2

Linked Data

• MyVariant Identifiers: chr3:g.49162486T>G (hg19) ; chr3:g.49125053T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125053T>G , CM000665.2:g.49125053T>G	GRCh38
NC_000003.11:g.49162486T>G , CM000665.1:g.49162486T>G	GRCh37
NC_000003.10:g.49137490T>G	NCBI36
NG_008094.1:g.13114A>C
NG_054716.1:g.886A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000305544.9:c.2837A>C MANE Select	ENSP00000307156.4:p.Asp946Ala
ENST00000305544.8:c.2837A>C	ENSP00000307156.4:p.Asp946Ala
ENST00000418109.5:c.2837A>C	ENSP00000388325.1:p.Asp946Ala
ENST00000462930.5:n.244A>C
ENST00000464891.5:n.570A>C
ENST00000483057.1:n.437A>C
ENST00000486298.5:n.542A>C
ENST00000542580.1:n.152A>C
NM_002292.3:c.2837A>C	NP_002283.3:p.Asp946Ala
XM_005265127.3:c.2837A>C	XP_005265184.1:p.Asp946Ala
XM_005265127.4:c.2837A>C	XP_005265184.1:p.Asp946Ala
NM_002292.4:c.2837A>C MANE Select	NP_002283.3:p.Asp946Ala