Canonical Allele Identifier: CA352745488
Gene: LAMB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49130824C>G , CM000665.2:g.49130824C>G GRCh38
NC_000003.11:g.49168257C>G , CM000665.1:g.49168257C>G GRCh37
NC_000003.10:g.49143261C>G NCBI36
NG_008094.1:g.7343G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000305544.9:c.952G>C MANE Select ENSP00000307156.4:p.Gly318Arg
ENST00000305544.8:c.952G>C ENSP00000307156.4:p.Gly318Arg
ENST00000418109.5:c.952G>C ENSP00000388325.1:p.Gly318Arg
NM_002292.3:c.952G>C NP_002283.3:p.Gly318Arg
XM_005265127.3:c.952G>C XP_005265184.1:p.Gly318Arg
XM_005265127.4:c.952G>C XP_005265184.1:p.Gly318Arg
NM_002292.4:c.952G>C MANE Select NP_002283.3:p.Gly318Arg