Canonical Allele Identifier: CA352694009

Gene: LAMB2

Linked Data

• gnomAD v4: 3-49122937-G-T
• MyVariant Identifiers: chr3:g.49160370G>T (hg19) ; chr3:g.49122937G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49122937G>T , CM000665.2:g.49122937G>T	GRCh38
NC_000003.11:g.49160370G>T , CM000665.1:g.49160370G>T	GRCh37
NC_000003.10:g.49135374G>T	NCBI36
NG_008094.1:g.15230C>A
NG_054716.1:g.3002C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.4340C>A MANE Select	ENSP00000307156.4:p.Ala1447Asp
ENST00000305544.8:c.4340C>A	ENSP00000307156.4:p.Ala1447Asp
ENST00000418109.5:c.4340C>A	ENSP00000388325.1:p.Ala1447Asp
ENST00000469665.1:n.649C>A
NM_002292.3:c.4340C>A	NP_002283.3:p.Ala1447Asp
XM_005265127.3:c.4340C>A	XP_005265184.1:p.Ala1447Asp
XM_005265127.4:c.4340C>A	XP_005265184.1:p.Ala1447Asp
NM_002292.4:c.4340C>A MANE Select	NP_002283.3:p.Ala1447Asp