Canonical Allele Identifier: CA1148427641

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209632739G= , CM000663.2:g.209632739G=	GRCh38
NC_000001.10:g.209806084G= , CM000663.1:g.209806084G=	GRCh37
NC_000001.9:g.207872707G=	NCBI36
NG_007116.1:g.24737C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.666C= MANE Select	ENSP00000348384.3:p.Thr222=
ENST00000356082.8:c.666C=	ENSP00000348384.3:p.Thr222=
ENST00000367030.7:c.666C=	ENSP00000355997.3:p.Thr222=
ENST00000391911.5:c.666C=	ENSP00000375778.1:p.Thr222=
NM_000228.2:c.666C=	NP_000219.2:p.Thr222=
NM_001017402.1:c.666C=	NP_001017402.1:p.Thr222=
NM_001127641.1:c.666C=	NP_001121113.1:p.Thr222=
XM_005273124.3:c.666C=	XP_005273181.1:p.Thr222=
XM_005273124.4:c.666C=	XP_005273181.1:p.Thr222=
XM_017001272.2:c.474C=	XP_016856761.1:p.Thr158=
NM_000228.3:c.666C= MANE Select	NP_000219.2:p.Thr222=
NM_001017402.2:c.666C=	NP_001017402.1:p.Thr222=