Canonical Allele Identifier: CA433834227

Gene: LAMB2

Linked Data

• MyVariant Identifiers: chr3:g.49162548C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125115C>G , CM000665.2:g.49125115C>G	GRCh38
NC_000003.11:g.49162548C>G , CM000665.1:g.49162548C>G	GRCh37
NC_000003.10:g.49137552C>G	NCBI36
NG_008094.1:g.13052G>C
NG_054716.1:g.824G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2775G>C MANE Select	ENSP00000307156.4:p.Arg925=
ENST00000305544.8:c.2775G>C	ENSP00000307156.4:p.Arg925=
ENST00000418109.5:c.2775G>C	ENSP00000388325.1:p.Arg925=
ENST00000462930.5:n.182G>C
ENST00000464891.5:n.508G>C
ENST00000483057.1:n.375G>C
ENST00000486298.5:n.480G>C
ENST00000542580.1:n.90G>C
NM_002292.3:c.2775G>C	NP_002283.3:p.Arg925=
XM_005265127.3:c.2775G>C	XP_005265184.1:p.Arg925=
XM_005265127.4:c.2775G>C	XP_005265184.1:p.Arg925=
NM_002292.4:c.2775G>C MANE Select	NP_002283.3:p.Arg925=