Canonical Allele Identifier: CA2484294935

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209615172T= , CM000663.2:g.209615172T=	GRCh38
NC_000001.10:g.209788517T= , CM000663.1:g.209788517T=	GRCh37
NC_000001.9:g.207855140T=	NCBI36
NG_007116.1:g.42304A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.*99A= MANE Select	ENSP00000348384.3:n.*99A=
ENST00000356082.8:c.*99A=	ENSP00000348384.3:n.*99A=
ENST00000367030.7:c.*99A=	ENSP00000355997.3:n.*99A=
ENST00000391911.5:c.*99A=	ENSP00000375778.1:n.*99A=
NM_000228.2:c.*99A=	NP_000219.2:n.*99A=
NM_001017402.1:c.*99A=	NP_001017402.1:n.*99A=
NM_001127641.1:c.*99A=	NP_001121113.1:n.*99A=
XM_005273124.3:c.*99A=	XP_005273181.1:n.*99A=
XM_005273124.4:c.*99A=	XP_005273181.1:n.*99A=
XM_017001272.2:c.*99A=	XP_016856761.1:n.*99A=
NM_000228.3:c.*99A= MANE Select	NP_000219.2:n.*99A=
NM_001017402.2:c.*99A=	NP_001017402.1:n.*99A=