Canonical Allele Identifier: CA433834445

Gene: LAMB2

Linked Data

• dbSNP Id: rs1441261598
• gnomAD v4: 3-49125399-C-A
• MyVariant Identifiers: chr3:g.49162832C>A (hg19) ; chr3:g.49125399C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125399C>A , CM000665.2:g.49125399C>A	GRCh38
NC_000003.11:g.49162832C>A , CM000665.1:g.49162832C>A	GRCh37
NC_000003.10:g.49137836C>A	NCBI36
NG_008094.1:g.12768G>T
NG_054716.1:g.540G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2574G>T MANE Select	ENSP00000307156.4:p.Gly858=
ENST00000305544.8:c.2574G>T	ENSP00000307156.4:p.Gly858=
ENST00000418109.5:c.2574G>T	ENSP00000388325.1:p.Gly858=
ENST00000464891.5:n.323G>T
ENST00000477701.1:n.447G>T
ENST00000483057.1:n.174G>T
ENST00000486298.5:n.426-230G>T
NM_002292.3:c.2574G>T	NP_002283.3:p.Gly858=
XM_005265127.3:c.2574G>T	XP_005265184.1:p.Gly858=
XM_005265127.4:c.2574G>T	XP_005265184.1:p.Gly858=
NM_002292.4:c.2574G>T MANE Select	NP_002283.3:p.Gly858=