Canonical Allele Identifier: CA344585174
Gene: LAMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209618564T>A , CM000663.2:g.209618564T>A GRCh38
NC_000001.10:g.209791909T>A , CM000663.1:g.209791909T>A GRCh37
NC_000001.9:g.207858532T>A NCBI36
NG_007116.1:g.38912A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000356082.9:c.2797A>T MANE Select ENSP00000348384.3:p.Asn933Tyr
ENST00000356082.8:c.2797A>T ENSP00000348384.3:p.Asn933Tyr
ENST00000367030.7:c.2797A>T ENSP00000355997.3:p.Asn933Tyr
ENST00000391911.5:c.2797A>T ENSP00000375778.1:p.Asn933Tyr
ENST00000455193.1:c.4A>T ENSP00000398683.1:p.Asn2Tyr
NM_000228.2:c.2797A>T NP_000219.2:p.Asn933Tyr
NM_001017402.1:c.2797A>T NP_001017402.1:p.Asn933Tyr
NM_001127641.1:c.2797A>T NP_001121113.1:p.Asn933Tyr
XM_005273124.3:c.2797A>T XP_005273181.1:p.Asn933Tyr
XM_005273124.4:c.2797A>T XP_005273181.1:p.Asn933Tyr
XM_017001272.2:c.2605A>T XP_016856761.1:p.Asn869Tyr
NM_000228.3:c.2797A>T MANE Select NP_000219.2:p.Asn933Tyr
NM_001017402.2:c.2797A>T NP_001017402.1:p.Asn933Tyr