Canonical Allele Identifier: CA1363342847
Gene: LAMB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49131129G= , CM000665.2:g.49131129G= GRCh38
NC_000003.11:g.49168562G= , CM000665.1:g.49168562G= GRCh37
NC_000003.10:g.49143566G= NCBI36
NG_008094.1:g.7038C=

Transcript Alleles

HGVS Amino-acid change
ENST00000305544.9:c.736C= MANE Select ENSP00000307156.4:p.Arg246=
ENST00000305544.8:c.736C= ENSP00000307156.4:p.Arg246=
ENST00000418109.5:c.736C= ENSP00000388325.1:p.Arg246=
ENST00000494831.1:c.289C= ENSP00000444751.1:p.Arg97=
NM_002292.3:c.736C= NP_002283.3:p.Arg246=
XM_005265127.3:c.736C= XP_005265184.1:p.Arg246=
XM_005265127.4:c.736C= XP_005265184.1:p.Arg246=
NM_002292.4:c.736C= MANE Select NP_002283.3:p.Arg246=