Canonical Allele Identifier: CA433634180

Gene: LAMB2

Linked Data

• MyVariant Identifiers: chr3:g.49160327T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49122894T>G , CM000665.2:g.49122894T>G	GRCh38
NC_000003.11:g.49160327T>G , CM000665.1:g.49160327T>G	GRCh37
NC_000003.10:g.49135331T>G	NCBI36
NG_008094.1:g.15273A>C
NG_054716.1:g.3045A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.4383A>C MANE Select	ENSP00000307156.4:p.Ala1461=
ENST00000305544.8:c.4383A>C	ENSP00000307156.4:p.Ala1461=
ENST00000418109.5:c.4383A>C	ENSP00000388325.1:p.Ala1461=
ENST00000469665.1:n.692A>C
NM_002292.3:c.4383A>C	NP_002283.3:p.Ala1461=
XM_005265127.3:c.4383A>C	XP_005265184.1:p.Ala1461=
XM_005265127.4:c.4383A>C	XP_005265184.1:p.Ala1461=
NM_002292.4:c.4383A>C MANE Select	NP_002283.3:p.Ala1461=