Canonical Allele Identifier: CA907805136

Gene: LAMB2

Linked Data

• dbSNP Id: rs1332913346
• MyVariant Identifiers: chr3:g.49160534C>A (hg19) ; chr3:g.49123101C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49123101C>A , CM000665.2:g.49123101C>A	GRCh38
NC_000003.11:g.49160534C>A , CM000665.1:g.49160534C>A	GRCh37
NC_000003.10:g.49135538C>A	NCBI36
NG_008094.1:g.15066G>T
NG_054716.1:g.2838G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.4224+31G>T MANE Select	ENSP00000307156.4:n.4224+31G>T
ENST00000305544.8:c.4224+31G>T	ENSP00000307156.4:n.4224+31G>T
ENST00000418109.5:c.4224+31G>T	ENSP00000388325.1:n.4224+31G>T
ENST00000469665.1:n.485G>T
NM_002292.3:c.4224+31G>T	NP_002283.3:n.4224+31G>T
XM_005265127.3:c.4224+31G>T	XP_005265184.1:n.4224+31G>T
XM_005265127.4:c.4224+31G>T	XP_005265184.1:n.4224+31G>T
NM_002292.4:c.4224+31G>T MANE Select	NP_002283.3:n.4224+31G>T