Canonical Allele Identifier: CA1363342650
Gene: LAMB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49130718T= , CM000665.2:g.49130718T= GRCh38
NC_000003.11:g.49168151T= , CM000665.1:g.49168151T= GRCh37
NC_000003.10:g.49143155T= NCBI36
NG_008094.1:g.7449A=

Transcript Alleles

HGVS Amino-acid change
ENST00000305544.9:c.1036+22A= MANE Select ENSP00000307156.4:n.1036+22A=
ENST00000305544.8:c.1036+22A= ENSP00000307156.4:n.1036+22A=
ENST00000418109.5:c.1036+22A= ENSP00000388325.1:n.1036+22A=
NM_002292.3:c.1036+22A= NP_002283.3:n.1036+22A=
XM_005265127.3:c.1036+22A= XP_005265184.1:n.1036+22A=
XM_005265127.4:c.1036+22A= XP_005265184.1:n.1036+22A=
NM_002292.4:c.1036+22A= MANE Select NP_002283.3:n.1036+22A=
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