Canonical Allele Identifier: CA2484309296

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209649913C= , CM000663.2:g.209649913C=	GRCh38
NC_000001.10:g.209823258C= , CM000663.1:g.209823258C=	GRCh37
NC_000001.9:g.207889881C=	NCBI36
NG_007116.1:g.7563G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.183+51G= MANE Select	ENSP00000348384.3:n.183+51G=
ENST00000356082.8:c.183+51G=	ENSP00000348384.3:n.183+51G=
ENST00000367030.7:c.183+51G=	ENSP00000355997.3:n.183+51G=
ENST00000391911.5:c.183+51G=	ENSP00000375778.1:n.183+51G=
ENST00000415782.1:c.183+51G=	ENSP00000388960.1:n.183+51G=
NM_000228.2:c.183+51G=	NP_000219.2:n.183+51G=
NM_001017402.1:c.183+51G=	NP_001017402.1:n.183+51G=
NM_001127641.1:c.183+51G=	NP_001121113.1:n.183+51G=
XM_005273124.3:c.183+51G=	XP_005273181.1:n.183+51G=
XM_005273124.4:c.183+51G=	XP_005273181.1:n.183+51G=
XM_017001272.2:c.183+51G=	XP_016856761.1:n.183+51G=
NM_000228.3:c.183+51G= MANE Select	NP_000219.2:n.183+51G=
NM_001017402.2:c.183+51G=	NP_001017402.1:n.183+51G=