Canonical Allele Identifier: CA2650321715
Gene: LAMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209624127dup , CM000663.2:g.209624127dup GRCh38
NC_000001.10:g.209797472dup , CM000663.1:g.209797472dup GRCh37
NC_000001.9:g.207864095dup NCBI36
NG_007116.1:g.33349dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.1977-127dup MANE Select ENSP00000348384.3:n.1977-127dup
ENST00000356082.8:c.1977-127dup ENSP00000348384.3:n.1977-127dup
ENST00000367030.7:c.1977-127dup ENSP00000355997.3:n.1977-127dup
ENST00000391911.5:c.1977-127dup ENSP00000375778.1:n.1977-127dup
NM_000228.2:c.1977-127dup NP_000219.2:n.1977-127dup
NM_001017402.1:c.1977-127dup NP_001017402.1:n.1977-127dup
NM_001127641.1:c.1977-127dup NP_001121113.1:n.1977-127dup
XM_005273124.3:c.1977-127dup XP_005273181.1:n.1977-127dup
XM_005273124.4:c.1977-127dup XP_005273181.1:n.1977-127dup
XM_017001272.2:c.1785-127dup XP_016856761.1:n.1785-127dup
NM_000228.3:c.1977-127dup MANE Select NP_000219.2:n.1977-127dup
NM_001017402.2:c.1977-127dup NP_001017402.1:n.1977-127dup