Canonical Allele Identifier: CA352747213
Gene: LAMB2 HGNC NCBI

Linked Data

dbSNP Id: rs2107644265

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49131038T>C , CM000665.2:g.49131038T>C GRCh38
NC_000003.11:g.49168471T>C , CM000665.1:g.49168471T>C GRCh37
NC_000003.10:g.49143475T>C NCBI36
NG_008094.1:g.7129A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000305544.9:c.827A>G MANE Select ENSP00000307156.4:p.Glu276Gly
ENST00000305544.8:c.827A>G ENSP00000307156.4:p.Glu276Gly
ENST00000418109.5:c.827A>G ENSP00000388325.1:p.Glu276Gly
ENST00000494831.1:c.380A>G ENSP00000444751.1:p.Glu127Gly
NM_002292.3:c.827A>G NP_002283.3:p.Glu276Gly
XM_005265127.3:c.827A>G XP_005265184.1:p.Glu276Gly
XM_005265127.4:c.827A>G XP_005265184.1:p.Glu276Gly
NM_002292.4:c.827A>G MANE Select NP_002283.3:p.Glu276Gly