Canonical Allele Identifier: CA543048641

Gene: LAMB2

Linked Data

• dbSNP Id: rs1289751635
• gnomAD v2: 3-49162922-G-A
• gnomAD v4: 3-49125489-G-A
• MyVariant Identifiers: chr3:g.49162922G>A (hg19) ; chr3:g.49125489G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49125489G>A , CM000665.2:g.49125489G>A	GRCh38
NC_000003.11:g.49162922G>A , CM000665.1:g.49162922G>A	GRCh37
NC_000003.10:g.49137926G>A	NCBI36
NG_008094.1:g.12678C>T
NG_054716.1:g.450C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.2489-5C>T MANE Select	ENSP00000307156.4:n.2489-5C>T
ENST00000305544.8:c.2489-5C>T	ENSP00000307156.4:n.2489-5C>T
ENST00000418109.5:c.2489-5C>T	ENSP00000388325.1:n.2489-5C>T
ENST00000464891.5:n.233C>T
ENST00000477701.1:n.362-5C>T
ENST00000483057.1:n.84C>T
ENST00000486298.5:n.426-320C>T
NM_002292.3:c.2489-5C>T	NP_002283.3:n.2489-5C>T
XM_005265127.3:c.2489-5C>T	XP_005265184.1:n.2489-5C>T
XM_005265127.4:c.2489-5C>T	XP_005265184.1:n.2489-5C>T
NM_002292.4:c.2489-5C>T MANE Select	NP_002283.3:n.2489-5C>T