Canonical Allele Identifier: CA2484295737

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209617161A= , CM000663.2:g.209617161A=	GRCh38
NC_000001.10:g.209790506A= , CM000663.1:g.209790506A=	GRCh37
NC_000001.9:g.207857129A=	NCBI36
NG_007116.1:g.40315T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.3228+249T= MANE Select	ENSP00000348384.3:n.3228+249T=
ENST00000356082.8:c.3228+249T=	ENSP00000348384.3:n.3228+249T=
ENST00000367030.7:c.3228+249T=	ENSP00000355997.3:n.3228+249T=
ENST00000391911.5:c.3228+249T=	ENSP00000375778.1:n.3228+249T=
ENST00000455193.1:c.435+249T=	ENSP00000398683.1:n.435+249T=
NM_000228.2:c.3228+249T=	NP_000219.2:n.3228+249T=
NM_001017402.1:c.3228+249T=	NP_001017402.1:n.3228+249T=
NM_001127641.1:c.3228+249T=	NP_001121113.1:n.3228+249T=
XM_005273124.3:c.3228+249T=	XP_005273181.1:n.3228+249T=
XM_005273124.4:c.3228+249T=	XP_005273181.1:n.3228+249T=
XM_017001272.2:c.3036+249T=	XP_016856761.1:n.3036+249T=
NM_000228.3:c.3228+249T= MANE Select	NP_000219.2:n.3228+249T=
NM_001017402.2:c.3228+249T=	NP_001017402.1:n.3228+249T=