Canonical Allele Identifier: CA2665695468
Gene: LAMB2 HGNC NCBI

Linked Data

gnomAD v4: 3-49123084-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49123084G>T , CM000665.2:g.49123084G>T GRCh38
NC_000003.11:g.49160517G>T , CM000665.1:g.49160517G>T GRCh37
NC_000003.10:g.49135521G>T NCBI36
NG_008094.1:g.15083C>A
NG_054716.1:g.2855C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.4225-32C>A MANE Select ENSP00000307156.4:n.4225-32C>A
ENST00000305544.8:c.4225-32C>A ENSP00000307156.4:n.4225-32C>A
ENST00000418109.5:c.4225-32C>A ENSP00000388325.1:n.4225-32C>A
ENST00000469665.1:n.502C>A
NM_002292.3:c.4225-32C>A NP_002283.3:n.4225-32C>A
XM_005265127.3:c.4225-32C>A XP_005265184.1:n.4225-32C>A
XM_005265127.4:c.4225-32C>A XP_005265184.1:n.4225-32C>A
NM_002292.4:c.4225-32C>A MANE Select NP_002283.3:n.4225-32C>A
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