Canonical Allele Identifier: CA2484294857

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209614974C= , CM000663.2:g.209614974C=	GRCh38
NC_000001.10:g.209788319C= , CM000663.1:g.209788319C=	GRCh37
NC_000001.9:g.207854942C=	NCBI36
NG_007116.1:g.42502G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.*297G= MANE Select	ENSP00000348384.3:n.*297G=
ENST00000356082.8:c.*297G=	ENSP00000348384.3:n.*297G=
ENST00000391911.5:c.*297G=	ENSP00000375778.1:n.*297G=
NM_000228.2:c.*297G=	NP_000219.2:n.*297G=
NM_001017402.1:c.*297G=	NP_001017402.1:n.*297G=
NM_001127641.1:c.*297G=	NP_001121113.1:n.*297G=
XM_005273124.3:c.*297G=	XP_005273181.1:n.*297G=
XM_005273124.4:c.*297G=	XP_005273181.1:n.*297G=
XM_017001272.2:c.*297G=	XP_016856761.1:n.*297G=
NM_000228.3:c.*297G= MANE Select	NP_000219.2:n.*297G=
NM_001017402.2:c.*297G=	NP_001017402.1:n.*297G=