Canonical Allele Identifier: CA352692889

Gene: LAMB2

Linked Data

• MyVariant Identifiers: chr3:g.49160271G>T (hg19) ; chr3:g.49122838G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49122838G>T , CM000665.2:g.49122838G>T	GRCh38
NC_000003.11:g.49160271G>T , CM000665.1:g.49160271G>T	GRCh37
NC_000003.10:g.49135275G>T	NCBI36
NG_008094.1:g.15329C>A
NG_054716.1:g.3101C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.4439C>A MANE Select	ENSP00000307156.4:p.Thr1480Asn
ENST00000305544.8:c.4439C>A	ENSP00000307156.4:p.Thr1480Asn
ENST00000418109.5:c.4439C>A	ENSP00000388325.1:p.Thr1480Asn
ENST00000469665.1:n.748C>A
NM_002292.3:c.4439C>A	NP_002283.3:p.Thr1480Asn
XM_005265127.3:c.4439C>A	XP_005265184.1:p.Thr1480Asn
XM_005265127.4:c.4439C>A	XP_005265184.1:p.Thr1480Asn
NM_002292.4:c.4439C>A MANE Select	NP_002283.3:p.Thr1480Asn