Canonical Allele Identifier: CA2484302183
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209633153A= , CM000663.2:g.209633153A= GRCh38
NC_000001.10:g.209806498A= , CM000663.1:g.209806498A= GRCh37
NC_000001.9:g.207873121A= NCBI36
NG_007116.1:g.24323T=

Transcript Alleles

HGVS Amino-acid change
ENST00000356082.9:c.565-20T= MANE Select ENSP00000348384.3:n.565-20T=
ENST00000356082.8:c.565-20T= ENSP00000348384.3:n.565-20T=
ENST00000367030.7:c.565-20T= ENSP00000355997.3:n.565-20T=
ENST00000391911.5:c.565-20T= ENSP00000375778.1:n.565-20T=
NM_000228.2:c.565-20T= NP_000219.2:n.565-20T=
NM_001017402.1:c.565-20T= NP_001017402.1:n.565-20T=
NM_001127641.1:c.565-20T= NP_001121113.1:n.565-20T=
XM_005273124.3:c.565-20T= XP_005273181.1:n.565-20T=
XM_005273124.4:c.565-20T= XP_005273181.1:n.565-20T=
XM_017001272.2:c.373-20T= XP_016856761.1:n.373-20T=
NM_000228.3:c.565-20T= MANE Select NP_000219.2:n.565-20T=
NM_001017402.2:c.565-20T= NP_001017402.1:n.565-20T=