Canonical Allele Identifier: CA2484298339

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209623699A= , CM000663.2:g.209623699A=	GRCh38
NC_000001.10:g.209797044A= , CM000663.1:g.209797044A=	GRCh37
NC_000001.9:g.207863667A=	NCBI36
NG_007116.1:g.33777T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.2164T= MANE Select	ENSP00000348384.3:p.Tyr722=
ENST00000356082.8:c.2164T=	ENSP00000348384.3:p.Tyr722=
ENST00000367030.7:c.2164T=	ENSP00000355997.3:p.Tyr722=
ENST00000391911.5:c.2164T=	ENSP00000375778.1:p.Tyr722=
NM_000228.2:c.2164T=	NP_000219.2:p.Tyr722=
NM_001017402.1:c.2164T=	NP_001017402.1:p.Tyr722=
NM_001127641.1:c.2164T=	NP_001121113.1:p.Tyr722=
XM_005273124.3:c.2164T=	XP_005273181.1:p.Tyr722=
XM_005273124.4:c.2164T=	XP_005273181.1:p.Tyr722=
XM_017001272.2:c.1972T=	XP_016856761.1:p.Tyr658=
NM_000228.3:c.2164T= MANE Select	NP_000219.2:p.Tyr722=
NM_001017402.2:c.2164T=	NP_001017402.1:p.Tyr722=