Canonical Allele Identifier: CA344584978
Gene: LAMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209618465C>T , CM000663.2:g.209618465C>T GRCh38
NC_000001.10:g.209791810C>T , CM000663.1:g.209791810C>T GRCh37
NC_000001.9:g.207858433C>T NCBI36
NG_007116.1:g.39011G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000356082.9:c.2896G>A MANE Select ENSP00000348384.3:p.Ala966Thr
ENST00000356082.8:c.2896G>A ENSP00000348384.3:p.Ala966Thr
ENST00000367030.7:c.2896G>A ENSP00000355997.3:p.Ala966Thr
ENST00000391911.5:c.2896G>A ENSP00000375778.1:p.Ala966Thr
ENST00000455193.1:c.103G>A ENSP00000398683.1:p.Ala35Thr
NM_000228.2:c.2896G>A NP_000219.2:p.Ala966Thr
NM_001017402.1:c.2896G>A NP_001017402.1:p.Ala966Thr
NM_001127641.1:c.2896G>A NP_001121113.1:p.Ala966Thr
XM_005273124.3:c.2896G>A XP_005273181.1:p.Ala966Thr
XM_005273124.4:c.2896G>A XP_005273181.1:p.Ala966Thr
XM_017001272.2:c.2704G>A XP_016856761.1:p.Ala902Thr
NM_000228.3:c.2896G>A MANE Select NP_000219.2:p.Ala966Thr
NM_001017402.2:c.2896G>A NP_001017402.1:p.Ala966Thr