Canonical Allele Identifier: CA1363343284
Gene: LAMB2 HGNC NCBI

Linked Data

dbSNP Id: rs2045487265
gnomAD v4: 3-49132067-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49132067T>C , CM000665.2:g.49132067T>C GRCh38
NC_000003.11:g.49169500T>C , CM000665.1:g.49169500T>C GRCh37
NC_000003.10:g.49144504T>C NCBI36
NG_008094.1:g.6100A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000305544.9:c.459+49A>G MANE Select ENSP00000307156.4:n.459+49A>G
ENST00000305544.8:c.459+49A>G ENSP00000307156.4:n.459+49A>G
ENST00000418109.5:c.459+49A>G ENSP00000388325.1:n.459+49A>G
ENST00000494831.1:c.12+49A>G ENSP00000444751.1:n.12+49A>G
NM_002292.3:c.459+49A>G NP_002283.3:n.459+49A>G
XM_005265127.3:c.459+49A>G XP_005265184.1:n.459+49A>G
XM_005265127.4:c.459+49A>G XP_005265184.1:n.459+49A>G
NM_002292.4:c.459+49A>G MANE Select NP_002283.3:n.459+49A>G
Search 100 bp 5'
Search 100 bp 3'