Canonical Allele Identifier: CA352747234
Gene: LAMB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49131039C>T , CM000665.2:g.49131039C>T GRCh38
NC_000003.11:g.49168472C>T , CM000665.1:g.49168472C>T GRCh37
NC_000003.10:g.49143476C>T NCBI36
NG_008094.1:g.7128G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000305544.9:c.826G>A MANE Select ENSP00000307156.4:p.Glu276Lys
ENST00000305544.8:c.826G>A ENSP00000307156.4:p.Glu276Lys
ENST00000418109.5:c.826G>A ENSP00000388325.1:p.Glu276Lys
ENST00000494831.1:c.379G>A ENSP00000444751.1:p.Glu127Lys
NM_002292.3:c.826G>A NP_002283.3:p.Glu276Lys
XM_005265127.3:c.826G>A XP_005265184.1:p.Glu276Lys
XM_005265127.4:c.826G>A XP_005265184.1:p.Glu276Lys
NM_002292.4:c.826G>A MANE Select NP_002283.3:p.Glu276Lys