Canonical Allele Identifier: CA1363342658
Gene: LAMB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49130735C= , CM000665.2:g.49130735C= GRCh38
NC_000003.11:g.49168168C= , CM000665.1:g.49168168C= GRCh37
NC_000003.10:g.49143172C= NCBI36
NG_008094.1:g.7432G=

Transcript Alleles

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