Canonical Allele Identifier: CA2484299626
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209626797C= , CM000663.2:g.209626797C= GRCh38
NC_000001.10:g.209800142C= , CM000663.1:g.209800142C= GRCh37
NC_000001.9:g.207866765C= NCBI36
NG_007116.1:g.30679G=

Transcript Alleles

HGVS Amino-acid change
ENST00000356082.9:c.1597+70G= MANE Select ENSP00000348384.3:n.1597+70G=
ENST00000356082.8:c.1597+70G= ENSP00000348384.3:n.1597+70G=
ENST00000367030.7:c.1597+70G= ENSP00000355997.3:n.1597+70G=
ENST00000391911.5:c.1597+70G= ENSP00000375778.1:n.1597+70G=
NM_000228.2:c.1597+70G= NP_000219.2:n.1597+70G=
NM_001017402.1:c.1597+70G= NP_001017402.1:n.1597+70G=
NM_001127641.1:c.1597+70G= NP_001121113.1:n.1597+70G=
XM_005273124.3:c.1597+70G= XP_005273181.1:n.1597+70G=
XM_005273124.4:c.1597+70G= XP_005273181.1:n.1597+70G=
XM_017001272.2:c.1405+70G= XP_016856761.1:n.1405+70G=
NM_000228.3:c.1597+70G= MANE Select NP_000219.2:n.1597+70G=
NM_001017402.2:c.1597+70G= NP_001017402.1:n.1597+70G=