Canonical Allele Identifier: CA1140304409

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209614979G= , CM000663.2:g.209614979G=	GRCh38
NC_000001.10:g.209788324G= , CM000663.1:g.209788324G=	GRCh37
NC_000001.9:g.207854947G=	NCBI36
NG_007116.1:g.42497C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.*292C= MANE Select	ENSP00000348384.3:n.*292C=
ENST00000356082.8:c.*292C=	ENSP00000348384.3:n.*292C=
ENST00000367030.7:c.*292C=	ENSP00000355997.3:n.*292C=
ENST00000391911.5:c.*292C=	ENSP00000375778.1:n.*292C=
NM_000228.2:c.*292C=	NP_000219.2:n.*292C=
NM_001017402.1:c.*292C=	NP_001017402.1:n.*292C=
NM_001127641.1:c.*292C=	NP_001121113.1:n.*292C=
XM_005273124.3:c.*292C=	XP_005273181.1:n.*292C=
XM_005273124.4:c.*292C=	XP_005273181.1:n.*292C=
XM_017001272.2:c.*292C=	XP_016856761.1:n.*292C=
NM_000228.3:c.*292C= MANE Select	NP_000219.2:n.*292C=
NM_001017402.2:c.*292C=	NP_001017402.1:n.*292C=