Canonical Allele Identifier: CA352692194
Gene: LAMB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49122775G>T , CM000665.2:g.49122775G>T GRCh38
NC_000003.11:g.49160208G>T , CM000665.1:g.49160208G>T GRCh37
NC_000003.10:g.49135212G>T NCBI36
NG_008094.1:g.15392C>A
NG_054716.1:g.3164C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.4502C>A MANE Select ENSP00000307156.4:p.Ser1501Tyr
ENST00000305544.8:c.4502C>A ENSP00000307156.4:p.Ser1501Tyr
ENST00000418109.5:c.4502C>A ENSP00000388325.1:p.Ser1501Tyr
ENST00000469665.1:n.811C>A
NM_002292.3:c.4502C>A NP_002283.3:p.Ser1501Tyr
XM_005265127.3:c.4502C>A XP_005265184.1:p.Ser1501Tyr
XM_005265127.4:c.4502C>A XP_005265184.1:p.Ser1501Tyr
NM_002292.4:c.4502C>A MANE Select NP_002283.3:p.Ser1501Tyr