Canonical Allele Identifier: CA352693392

Gene: LAMB2

Linked Data

• MyVariant Identifiers: chr3:g.49160316C>A (hg19) ; chr3:g.49122883C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49122883C>A , CM000665.2:g.49122883C>A	GRCh38
NC_000003.11:g.49160316C>A , CM000665.1:g.49160316C>A	GRCh37
NC_000003.10:g.49135320C>A	NCBI36
NG_008094.1:g.15284G>T
NG_054716.1:g.3056G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.4394G>T MANE Select	ENSP00000307156.4:p.Arg1465Leu
ENST00000305544.8:c.4394G>T	ENSP00000307156.4:p.Arg1465Leu
ENST00000418109.5:c.4394G>T	ENSP00000388325.1:p.Arg1465Leu
ENST00000469665.1:n.703G>T
NM_002292.3:c.4394G>T	NP_002283.3:p.Arg1465Leu
XM_005265127.3:c.4394G>T	XP_005265184.1:p.Arg1465Leu
XM_005265127.4:c.4394G>T	XP_005265184.1:p.Arg1465Leu
NM_002292.4:c.4394G>T MANE Select	NP_002283.3:p.Arg1465Leu