Canonical Allele Identifier: CA352748557
Gene: LAMB2 HGNC NCBI

Linked Data

dbSNP Id: rs1301449943

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49131142C>A , CM000665.2:g.49131142C>A GRCh38
NC_000003.11:g.49168575C>A , CM000665.1:g.49168575C>A GRCh37
NC_000003.10:g.49143579C>A NCBI36
NG_008094.1:g.7025G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000305544.9:c.723G>T MANE Select ENSP00000307156.4:p.Lys241Asn
ENST00000305544.8:c.723G>T ENSP00000307156.4:p.Lys241Asn
ENST00000418109.5:c.723G>T ENSP00000388325.1:p.Lys241Asn
ENST00000494831.1:c.276G>T ENSP00000444751.1:p.Lys92Asn
NM_002292.3:c.723G>T NP_002283.3:p.Lys241Asn
XM_005265127.3:c.723G>T XP_005265184.1:p.Lys241Asn
XM_005265127.4:c.723G>T XP_005265184.1:p.Lys241Asn
NM_002292.4:c.723G>T MANE Select NP_002283.3:p.Lys241Asn