Canonical Allele Identifier: CA2747561639
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209615380_209615409del , CM000663.2:g.209615380_209615409del GRCh38
NC_000001.10:g.209788725_209788754del , CM000663.1:g.209788725_209788754del GRCh37
NC_000001.9:g.207855348_207855377del NCBI36
NG_007116.1:g.42067_42096del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.3383-2_3410del
ENST00000356082.8:c.3383-2_3410del
ENST00000367030.7:c.3383-2_3410del
ENST00000391911.5:c.3383-2_3410del
NM_000228.2:c.3383-2_3410del
NM_001017402.1:c.3383-2_3410del
NM_001127641.1:c.3383-2_3410del
XM_005273124.3:c.3383-2_3410del
XM_005273124.4:c.3383-2_3410del
XM_017001272.2:c.3191-2_3218del
NM_000228.3:c.3383-2_3410del
NM_001017402.2:c.3383-2_3410del