Canonical Allele Identifier: CA1363339942
Gene: LAMB2 HGNC NCBI

Linked Data

dbSNP Id: rs2045367111
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49123087A>G , CM000665.2:g.49123087A>G GRCh38
NC_000003.11:g.49160520A>G , CM000665.1:g.49160520A>G GRCh37
NC_000003.10:g.49135524A>G NCBI36
NG_008094.1:g.15080T>C
NG_054716.1:g.2852T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.4225-35T>C MANE Select ENSP00000307156.4:n.4225-35T>C
ENST00000305544.8:c.4225-35T>C ENSP00000307156.4:n.4225-35T>C
ENST00000418109.5:c.4225-35T>C ENSP00000388325.1:n.4225-35T>C
ENST00000469665.1:n.499T>C
NM_002292.3:c.4225-35T>C NP_002283.3:n.4225-35T>C
XM_005265127.3:c.4225-35T>C XP_005265184.1:n.4225-35T>C
XM_005265127.4:c.4225-35T>C XP_005265184.1:n.4225-35T>C
NM_002292.4:c.4225-35T>C MANE Select NP_002283.3:n.4225-35T>C
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