Canonical Allele Identifier: CA2484294945
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209615198T= , CM000663.2:g.209615198T= GRCh38
NC_000001.10:g.209788543T= , CM000663.1:g.209788543T= GRCh37
NC_000001.9:g.207855166T= NCBI36
NG_007116.1:g.42278A=

Transcript Alleles

HGVS Amino-acid change
ENST00000356082.9:c.*73A= MANE Select ENSP00000348384.3:n.*73A=
ENST00000356082.8:c.*73A= ENSP00000348384.3:n.*73A=
ENST00000367030.7:c.*73A= ENSP00000355997.3:n.*73A=
ENST00000391911.5:c.*73A= ENSP00000375778.1:n.*73A=
NM_000228.2:c.*73A= NP_000219.2:n.*73A=
NM_001017402.1:c.*73A= NP_001017402.1:n.*73A=
NM_001127641.1:c.*73A= NP_001121113.1:n.*73A=
XM_005273124.3:c.*73A= XP_005273181.1:n.*73A=
XM_005273124.4:c.*73A= XP_005273181.1:n.*73A=
XM_017001272.2:c.*73A= XP_016856761.1:n.*73A=
NM_000228.3:c.*73A= MANE Select NP_000219.2:n.*73A=
NM_001017402.2:c.*73A= NP_001017402.1:n.*73A=