Canonical Allele Identifier: CA352716439

Gene: LAMB2

Linked Data

• MyVariant Identifiers: chr3:g.49162507A>T (hg19) ; chr3:g.49125074A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125074A>T , CM000665.2:g.49125074A>T	GRCh38
NC_000003.11:g.49162507A>T , CM000665.1:g.49162507A>T	GRCh37
NC_000003.10:g.49137511A>T	NCBI36
NG_008094.1:g.13093T>A
NG_054716.1:g.865T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2816T>A MANE Select	ENSP00000307156.4:p.Phe939Tyr
ENST00000305544.8:c.2816T>A	ENSP00000307156.4:p.Phe939Tyr
ENST00000418109.5:c.2816T>A	ENSP00000388325.1:p.Phe939Tyr
ENST00000462930.5:n.223T>A
ENST00000464891.5:n.549T>A
ENST00000483057.1:n.416T>A
ENST00000486298.5:n.521T>A
ENST00000542580.1:n.131T>A
NM_002292.3:c.2816T>A	NP_002283.3:p.Phe939Tyr
XM_005265127.3:c.2816T>A	XP_005265184.1:p.Phe939Tyr
XM_005265127.4:c.2816T>A	XP_005265184.1:p.Phe939Tyr
NM_002292.4:c.2816T>A MANE Select	NP_002283.3:p.Phe939Tyr