Canonical Allele Identifier: CA1144144129

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209617577C= , CM000663.2:g.209617577C=	GRCh38
NC_000001.10:g.209790922C= , CM000663.1:g.209790922C=	GRCh37
NC_000001.9:g.207857545C=	NCBI36
NG_007116.1:g.39899G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.3061G= MANE Select	ENSP00000348384.3:p.Val1021=
ENST00000356082.8:c.3061G=	ENSP00000348384.3:p.Val1021=
ENST00000367030.7:c.3061G=	ENSP00000355997.3:p.Val1021=
ENST00000391911.5:c.3061G=	ENSP00000375778.1:p.Val1021=
ENST00000455193.1:c.268G=	ENSP00000398683.1:p.Val90=
NM_000228.2:c.3061G=	NP_000219.2:p.Val1021=
NM_001017402.1:c.3061G=	NP_001017402.1:p.Val1021=
NM_001127641.1:c.3061G=	NP_001121113.1:p.Val1021=
XM_005273124.3:c.3061G=	XP_005273181.1:p.Val1021=
XM_005273124.4:c.3061G=	XP_005273181.1:p.Val1021=
XM_017001272.2:c.2869G=	XP_016856761.1:p.Val957=
NM_000228.3:c.3061G= MANE Select	NP_000219.2:p.Val1021=
NM_001017402.2:c.3061G=	NP_001017402.1:p.Val1021=