Canonical Allele Identifier: CA2484309213

Gene: LAMB3

Linked Data

• dbSNP Id: rs2076548041

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209649696_209649700del , CM000663.2:g.209649696_209649700del	GRCh38
NC_000001.10:g.209823041_209823045del , CM000663.1:g.209823041_209823045del	GRCh37
NC_000001.9:g.207889664_207889668del	NCBI36
NG_007116.1:g.7776_7780del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.183+264_183+268del MANE Select	ENSP00000348384.3:n.183+264_183+268del
ENST00000356082.8:c.183+264_183+268del	ENSP00000348384.3:n.183+264_183+268del
ENST00000367030.7:c.183+264_183+268del	ENSP00000355997.3:n.183+264_183+268del
ENST00000391911.5:c.183+264_183+268del	ENSP00000375778.1:n.183+264_183+268del
ENST00000415782.1:c.183+264_183+268del	ENSP00000388960.1:n.183+264_183+268del
NM_000228.2:c.183+264_183+268del	NP_000219.2:n.183+264_183+268del
NM_001017402.1:c.183+264_183+268del	NP_001017402.1:n.183+264_183+268del
NM_001127641.1:c.183+264_183+268del	NP_001121113.1:n.183+264_183+268del
XM_005273124.3:c.183+264_183+268del	XP_005273181.1:n.183+264_183+268del
XM_005273124.4:c.183+264_183+268del	XP_005273181.1:n.183+264_183+268del
XM_017001272.2:c.183+264_183+268del	XP_016856761.1:n.183+264_183+268del
NM_000228.3:c.183+264_183+268del MANE Select	NP_000219.2:n.183+264_183+268del
NM_001017402.2:c.183+264_183+268del	NP_001017402.1:n.183+264_183+268del