Canonical Allele Identifier: CA352694495
Gene: LAMB2 HGNC NCBI

Linked Data

gnomAD v4: 3-49122989-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49122989C>A , CM000665.2:g.49122989C>A GRCh38
NC_000003.11:g.49160422C>A , CM000665.1:g.49160422C>A GRCh37
NC_000003.10:g.49135426C>A NCBI36
NG_008094.1:g.15178G>T
NG_054716.1:g.2950G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.4288G>T MANE Select ENSP00000307156.4:p.Asp1430Tyr
ENST00000305544.8:c.4288G>T ENSP00000307156.4:p.Asp1430Tyr
ENST00000418109.5:c.4288G>T ENSP00000388325.1:p.Asp1430Tyr
ENST00000469665.1:n.597G>T
NM_002292.3:c.4288G>T NP_002283.3:p.Asp1430Tyr
XM_005265127.3:c.4288G>T XP_005265184.1:p.Asp1430Tyr
XM_005265127.4:c.4288G>T XP_005265184.1:p.Asp1430Tyr
NM_002292.4:c.4288G>T MANE Select NP_002283.3:p.Asp1430Tyr