Canonical Allele Identifier: CA1363342708

Gene: LAMB2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49130845T= , CM000665.2:g.49130845T=	GRCh38
NC_000003.11:g.49168278T= , CM000665.1:g.49168278T=	GRCh37
NC_000003.10:g.49143282T=	NCBI36
NG_008094.1:g.7322A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305544.9:c.931A= MANE Select	ENSP00000307156.4:p.Ile311=
ENST00000305544.8:c.931A=	ENSP00000307156.4:p.Ile311=
ENST00000418109.5:c.931A=	ENSP00000388325.1:p.Ile311=
NM_002292.3:c.931A=	NP_002283.3:p.Ile311=
XM_005265127.3:c.931A=	XP_005265184.1:p.Ile311=
XM_005265127.4:c.931A=	XP_005265184.1:p.Ile311=
NM_002292.4:c.931A= MANE Select	NP_002283.3:p.Ile311=