Canonical Allele Identifier: CA2650322124
Gene: LAMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209626794A>C , CM000663.2:g.209626794A>C GRCh38
NC_000001.10:g.209800139A>C , CM000663.1:g.209800139A>C GRCh37
NC_000001.9:g.207866762A>C NCBI36
NG_007116.1:g.30682T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.1597+73T>G MANE Select ENSP00000348384.3:n.1597+73T>G
ENST00000356082.8:c.1597+73T>G ENSP00000348384.3:n.1597+73T>G
ENST00000367030.7:c.1597+73T>G ENSP00000355997.3:n.1597+73T>G
ENST00000391911.5:c.1597+73T>G ENSP00000375778.1:n.1597+73T>G
NM_000228.2:c.1597+73T>G NP_000219.2:n.1597+73T>G
NM_001017402.1:c.1597+73T>G NP_001017402.1:n.1597+73T>G
NM_001127641.1:c.1597+73T>G NP_001121113.1:n.1597+73T>G
XM_005273124.3:c.1597+73T>G XP_005273181.1:n.1597+73T>G
XM_005273124.4:c.1597+73T>G XP_005273181.1:n.1597+73T>G
XM_017001272.2:c.1405+73T>G XP_016856761.1:n.1405+73T>G
NM_000228.3:c.1597+73T>G MANE Select NP_000219.2:n.1597+73T>G
NM_001017402.2:c.1597+73T>G NP_001017402.1:n.1597+73T>G