Canonical Allele Identifier: CA1363339956
Gene: LAMB2 HGNC NCBI

Linked Data

dbSNP Id: rs1236877102

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49123099A>C , CM000665.2:g.49123099A>C GRCh38
NC_000003.11:g.49160532A>C , CM000665.1:g.49160532A>C GRCh37
NC_000003.10:g.49135536A>C NCBI36
NG_008094.1:g.15068T>G
NG_054716.1:g.2840T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305544.9:c.4224+33T>G MANE Select ENSP00000307156.4:n.4224+33T>G
ENST00000305544.8:c.4224+33T>G ENSP00000307156.4:n.4224+33T>G
ENST00000418109.5:c.4224+33T>G ENSP00000388325.1:n.4224+33T>G
ENST00000469665.1:n.487T>G
NM_002292.3:c.4224+33T>G NP_002283.3:n.4224+33T>G
XM_005265127.3:c.4224+33T>G XP_005265184.1:n.4224+33T>G
XM_005265127.4:c.4224+33T>G XP_005265184.1:n.4224+33T>G
NM_002292.4:c.4224+33T>G MANE Select NP_002283.3:n.4224+33T>G