Canonical Allele Identifier: CA352747253
Gene: LAMB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49131041T>A , CM000665.2:g.49131041T>A GRCh38
NC_000003.11:g.49168474T>A , CM000665.1:g.49168474T>A GRCh37
NC_000003.10:g.49143478T>A NCBI36
NG_008094.1:g.7126A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000305544.9:c.824A>T MANE Select ENSP00000307156.4:p.Tyr275Phe
ENST00000305544.8:c.824A>T ENSP00000307156.4:p.Tyr275Phe
ENST00000418109.5:c.824A>T ENSP00000388325.1:p.Tyr275Phe
ENST00000494831.1:c.377A>T ENSP00000444751.1:p.Tyr126Phe
NM_002292.3:c.824A>T NP_002283.3:p.Tyr275Phe
XM_005265127.3:c.824A>T XP_005265184.1:p.Tyr275Phe
XM_005265127.4:c.824A>T XP_005265184.1:p.Tyr275Phe
NM_002292.4:c.824A>T MANE Select NP_002283.3:p.Tyr275Phe