Canonical Allele Identifier: CA352720400

Gene: LAMB2

Linked Data

• MyVariant Identifiers: chr3:g.49162866C>A (hg19) ; chr3:g.49125433C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125433C>A , CM000665.2:g.49125433C>A	GRCh38
NC_000003.11:g.49162866C>A , CM000665.1:g.49162866C>A	GRCh37
NC_000003.10:g.49137870C>A	NCBI36
NG_008094.1:g.12734G>T
NG_054716.1:g.506G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2540G>T MANE Select	ENSP00000307156.4:p.Ser847Ile
ENST00000305544.8:c.2540G>T	ENSP00000307156.4:p.Ser847Ile
ENST00000418109.5:c.2540G>T	ENSP00000388325.1:p.Ser847Ile
ENST00000464891.5:n.289G>T
ENST00000477701.1:n.413G>T
ENST00000483057.1:n.140G>T
ENST00000486298.5:n.426-264G>T
NM_002292.3:c.2540G>T	NP_002283.3:p.Ser847Ile
XM_005265127.3:c.2540G>T	XP_005265184.1:p.Ser847Ile
XM_005265127.4:c.2540G>T	XP_005265184.1:p.Ser847Ile
NM_002292.4:c.2540G>T MANE Select	NP_002283.3:p.Ser847Ile