Canonical Allele Identifier: CA352717592

Gene: LAMB2

Linked Data

• MyVariant Identifiers: chr3:g.49162601A>G (hg19) ; chr3:g.49125168A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125168A>G , CM000665.2:g.49125168A>G	GRCh38
NC_000003.11:g.49162601A>G , CM000665.1:g.49162601A>G	GRCh37
NC_000003.10:g.49137605A>G	NCBI36
NG_008094.1:g.12999T>C
NG_054716.1:g.771T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2722T>C MANE Select	ENSP00000307156.4:p.Cys908Arg
ENST00000305544.8:c.2722T>C	ENSP00000307156.4:p.Cys908Arg
ENST00000418109.5:c.2722T>C	ENSP00000388325.1:p.Cys908Arg
ENST00000462930.5:n.129T>C
ENST00000464891.5:n.455T>C
ENST00000483057.1:n.322T>C
ENST00000486298.5:n.427T>C
ENST00000542580.1:n.37T>C
NM_002292.3:c.2722T>C	NP_002283.3:p.Cys908Arg
XM_005265127.3:c.2722T>C	XP_005265184.1:p.Cys908Arg
XM_005265127.4:c.2722T>C	XP_005265184.1:p.Cys908Arg
NM_002292.4:c.2722T>C MANE Select	NP_002283.3:p.Cys908Arg