Canonical Allele Identifier: CA433834278

Gene: LAMB2

Linked Data

• dbSNP Id: rs2107639307
• MyVariant Identifiers: chr3:g.49162566T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125133T>C , CM000665.2:g.49125133T>C	GRCh38
NC_000003.11:g.49162566T>C , CM000665.1:g.49162566T>C	GRCh37
NC_000003.10:g.49137570T>C	NCBI36
NG_008094.1:g.13034A>G
NG_054716.1:g.806A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2757A>G MANE Select	ENSP00000307156.4:p.Pro919=
ENST00000305544.8:c.2757A>G	ENSP00000307156.4:p.Pro919=
ENST00000418109.5:c.2757A>G	ENSP00000388325.1:p.Pro919=
ENST00000462930.5:n.164A>G
ENST00000464891.5:n.490A>G
ENST00000483057.1:n.357A>G
ENST00000486298.5:n.462A>G
ENST00000542580.1:n.72A>G
NM_002292.3:c.2757A>G	NP_002283.3:p.Pro919=
XM_005265127.3:c.2757A>G	XP_005265184.1:p.Pro919=
XM_005265127.4:c.2757A>G	XP_005265184.1:p.Pro919=
NM_002292.4:c.2757A>G MANE Select	NP_002283.3:p.Pro919=