Canonical Allele Identifier: CA1363342850
Gene: LAMB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49131141T= , CM000665.2:g.49131141T= GRCh38
NC_000003.11:g.49168574T= , CM000665.1:g.49168574T= GRCh37
NC_000003.10:g.49143578T= NCBI36
NG_008094.1:g.7026A=

Transcript Alleles

HGVS Amino-acid change
ENST00000305544.9:c.724A= MANE Select ENSP00000307156.4:p.Ile242=
ENST00000305544.8:c.724A= ENSP00000307156.4:p.Ile242=
ENST00000418109.5:c.724A= ENSP00000388325.1:p.Ile242=
ENST00000494831.1:c.277A= ENSP00000444751.1:p.Ile93=
NM_002292.3:c.724A= NP_002283.3:p.Ile242=
XM_005265127.3:c.724A= XP_005265184.1:p.Ile242=
XM_005265127.4:c.724A= XP_005265184.1:p.Ile242=
NM_002292.4:c.724A= MANE Select NP_002283.3:p.Ile242=