Canonical Allele Identifier: CA2697962407
Gene: LAMB3 HGNC NCBI

Linked Data

dbSNP Id: rs2102407088

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209618662_209618663insTTAGGAAGTCCCGGACCTGCTGGATCAGGAGCCGT , CM000663.2:g.209618662_209618663insTTAGGAAGTCCCGGACCTGCTGGATCAGGAGCCGT GRCh38
NC_000001.10:g.209792007_209792008insTTAGGAAGTCCCGGACCTGCTGGATCAGGAGCCGT , CM000663.1:g.209792007_209792008insTTAGGAAGTCCCGGACCTGCTGGATCAGGAGCCGT GRCh37
NC_000001.9:g.207858630_207858631insTTAGGAAGTCCCGGACCTGCTGGATCAGGAGCCGT NCBI36
NG_007116.1:g.38813_38814insACGGCTCCTGATCCAGCAGGTCCGGGACTTCCTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGACTTCCTAA MANE Select ENSP00000348384.3:n.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGG...
ENST00000356082.8:c.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGACTTCCTAA ENSP00000348384.3:n.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGG...
ENST00000367030.7:c.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGACTTCCTAA ENSP00000355997.3:n.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGG...
ENST00000391911.5:c.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGACTTCCTAA ENSP00000375778.1:n.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGG...
ENST00000455193.1:c.-96_-95insACGGCTCCTGATCCAGCAGGTCCGGGACTTCCTAA ENSP00000398683.1:n.-96_-95insACGGCTCCTGATCCAGCAGGTCCGGGACTTC...
NM_000228.2:c.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGACTTCCTAA NP_000219.2:n.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGACTTC...
NM_001017402.1:c.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGACTTCCTAA NP_001017402.1:n.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGAC...
NM_001127641.1:c.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGACTTCCTAA NP_001121113.1:n.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGAC...
XM_005273124.3:c.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGACTTCCTAA XP_005273181.1:n.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGAC...
XM_005273124.4:c.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGACTTCCTAA XP_005273181.1:n.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGAC...
XM_017001272.2:c.2510-4_2510-3insACGGCTCCTGATCCAGCAGGTCCGGGACTTCCTAA XP_016856761.1:n.2510-4_2510-3insACGGCTCCTGATCCAGCAGGTCCGGGAC...
NM_000228.3:c.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGACTTCCTAA MANE Select NP_000219.2:n.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGACTTC...
NM_001017402.2:c.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGACTTCCTAA NP_001017402.1:n.2702-4_2702-3insACGGCTCCTGATCCAGCAGGTCCGGGAC...