Canonical Allele Identifier: CA352747201
Gene: LAMB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49131036G>T , CM000665.2:g.49131036G>T GRCh38
NC_000003.11:g.49168469G>T , CM000665.1:g.49168469G>T GRCh37
NC_000003.10:g.49143473G>T NCBI36
NG_008094.1:g.7131C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000305544.9:c.829C>A MANE Select ENSP00000307156.4:p.Leu277Met
ENST00000305544.8:c.829C>A ENSP00000307156.4:p.Leu277Met
ENST00000418109.5:c.829C>A ENSP00000388325.1:p.Leu277Met
ENST00000494831.1:c.382C>A ENSP00000444751.1:p.Leu128Met
NM_002292.3:c.829C>A NP_002283.3:p.Leu277Met
XM_005265127.3:c.829C>A XP_005265184.1:p.Leu277Met
XM_005265127.4:c.829C>A XP_005265184.1:p.Leu277Met
NM_002292.4:c.829C>A MANE Select NP_002283.3:p.Leu277Met