Canonical Allele Identifier: CA433834193

Gene: LAMB2

Linked Data

• MyVariant Identifiers: chr3:g.49162539G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125106G>C , CM000665.2:g.49125106G>C	GRCh38
NC_000003.11:g.49162539G>C , CM000665.1:g.49162539G>C	GRCh37
NC_000003.10:g.49137543G>C	NCBI36
NG_008094.1:g.13061C>G
NG_054716.1:g.833C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2784C>G MANE Select	ENSP00000307156.4:p.Pro928=
ENST00000305544.8:c.2784C>G	ENSP00000307156.4:p.Pro928=
ENST00000418109.5:c.2784C>G	ENSP00000388325.1:p.Pro928=
ENST00000462930.5:n.191C>G
ENST00000464891.5:n.517C>G
ENST00000483057.1:n.384C>G
ENST00000486298.5:n.489C>G
ENST00000542580.1:n.99C>G
NM_002292.3:c.2784C>G	NP_002283.3:p.Pro928=
XM_005265127.3:c.2784C>G	XP_005265184.1:p.Pro928=
XM_005265127.4:c.2784C>G	XP_005265184.1:p.Pro928=
NM_002292.4:c.2784C>G MANE Select	NP_002283.3:p.Pro928=