Canonical Allele Identifier: CA74480665

Gene: LAMB2

Linked Data

• dbSNP Id: rs987582385
• gnomAD v2: 3-49162683-C-T
• gnomAD v4: 3-49125250-C-T
• MyVariant Identifiers: chr3:g.49162683C>T (hg19) ; chr3:g.49125250C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125250C>T , CM000665.2:g.49125250C>T	GRCh38
NC_000003.11:g.49162683C>T , CM000665.1:g.49162683C>T	GRCh37
NC_000003.10:g.49137687C>T	NCBI36
NG_008094.1:g.12917G>A
NG_054716.1:g.689G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2720+3G>A MANE Select	ENSP00000307156.4:n.2720+3G>A
ENST00000305544.8:c.2720+3G>A	ENSP00000307156.4:n.2720+3G>A
ENST00000418109.5:c.2720+3G>A	ENSP00000388325.1:n.2720+3G>A
ENST00000462930.5:n.127+3G>A
ENST00000464891.5:n.453+19G>A
ENST00000483057.1:n.320+3G>A
ENST00000486298.5:n.426-81G>A
NM_002292.3:c.2720+3G>A	NP_002283.3:n.2720+3G>A
XM_005265127.3:c.2720+3G>A	XP_005265184.1:n.2720+3G>A
XM_005265127.4:c.2720+3G>A	XP_005265184.1:n.2720+3G>A
NM_002292.4:c.2720+3G>A MANE Select	NP_002283.3:n.2720+3G>A