Canonical Allele Identifier: CA352716774

Gene: LAMB2

Linked Data

• MyVariant Identifiers: chr3:g.49162532C>G (hg19) ; chr3:g.49125099C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125099C>G , CM000665.2:g.49125099C>G	GRCh38
NC_000003.11:g.49162532C>G , CM000665.1:g.49162532C>G	GRCh37
NC_000003.10:g.49137536C>G	NCBI36
NG_008094.1:g.13068G>C
NG_054716.1:g.840G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2791G>C MANE Select	ENSP00000307156.4:p.Glu931Gln
ENST00000305544.8:c.2791G>C	ENSP00000307156.4:p.Glu931Gln
ENST00000418109.5:c.2791G>C	ENSP00000388325.1:p.Glu931Gln
ENST00000462930.5:n.198G>C
ENST00000464891.5:n.524G>C
ENST00000483057.1:n.391G>C
ENST00000486298.5:n.496G>C
ENST00000542580.1:n.106G>C
NM_002292.3:c.2791G>C	NP_002283.3:p.Glu931Gln
XM_005265127.3:c.2791G>C	XP_005265184.1:p.Glu931Gln
XM_005265127.4:c.2791G>C	XP_005265184.1:p.Glu931Gln
NM_002292.4:c.2791G>C MANE Select	NP_002283.3:p.Glu931Gln