Canonical Allele Identifier: CA2394244

Gene: LAMB2

Linked Data

• dbSNP Id: rs781530275
• ExAC: 3:49162704 C / A
• gnomAD v2: 3-49162704-C-A
• gnomAD v3: 3-49125271-C-A
• gnomAD v4: 3-49125271-C-A
• MyVariant Identifiers: chr3:g.49162704C>A (hg19) ; chr3:g.49162704_49162706delinsACT (hg19) ; chr3:g.49125271C>A (hg38) ; chr3:g.49125271_49125273delinsACT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125271C>A , CM000665.2:g.49125271C>A	GRCh38
NC_000003.11:g.49162704C>A , CM000665.1:g.49162704C>A	GRCh37
NC_000003.10:g.49137708C>A	NCBI36
NG_008094.1:g.12896G>T
NG_054716.1:g.668G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2702G>T MANE Select	ENSP00000307156.4:p.Gly901Val
ENST00000305544.8:c.2702G>T	ENSP00000307156.4:p.Gly901Val
ENST00000418109.5:c.2702G>T	ENSP00000388325.1:p.Gly901Val
ENST00000462930.5:n.109G>T
ENST00000464891.5:n.451G>T
ENST00000483057.1:n.302G>T
ENST00000486298.5:n.426-102G>T
NM_002292.3:c.2702G>T	NP_002283.3:p.Gly901Val
XM_005265127.3:c.2702G>T	XP_005265184.1:p.Gly901Val
XM_005265127.4:c.2702G>T	XP_005265184.1:p.Gly901Val
NM_002292.4:c.2702G>T MANE Select	NP_002283.3:p.Gly901Val