Canonical Allele Identifier: CA2484296302
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209618582T= , CM000663.2:g.209618582T= GRCh38
NC_000001.10:g.209791927T= , CM000663.1:g.209791927T= GRCh37
NC_000001.9:g.207858550T= NCBI36
NG_007116.1:g.38894A=

Transcript Alleles

HGVS Amino-acid change
ENST00000356082.9:c.2779A= MANE Select ENSP00000348384.3:p.Thr927=
ENST00000356082.8:c.2779A= ENSP00000348384.3:p.Thr927=
ENST00000367030.7:c.2779A= ENSP00000355997.3:p.Thr927=
ENST00000391911.5:c.2779A= ENSP00000375778.1:p.Thr927=
ENST00000455193.1:c.-15A= ENSP00000398683.1:n.-15A=
NM_000228.2:c.2779A= NP_000219.2:p.Thr927=
NM_001017402.1:c.2779A= NP_001017402.1:p.Thr927=
NM_001127641.1:c.2779A= NP_001121113.1:p.Thr927=
XM_005273124.3:c.2779A= XP_005273181.1:p.Thr927=
XM_005273124.4:c.2779A= XP_005273181.1:p.Thr927=
XM_017001272.2:c.2587A= XP_016856761.1:p.Thr863=
NM_000228.3:c.2779A= MANE Select NP_000219.2:p.Thr927=
NM_001017402.2:c.2779A= NP_001017402.1:p.Thr927=