Canonical Allele Identifier: CA344585008
Gene: LAMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209618479C>A , CM000663.2:g.209618479C>A GRCh38
NC_000001.10:g.209791824C>A , CM000663.1:g.209791824C>A GRCh37
NC_000001.9:g.207858447C>A NCBI36
NG_007116.1:g.38997G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.2882G>T MANE Select ENSP00000348384.3:p.Arg961Leu
ENST00000356082.8:c.2882G>T ENSP00000348384.3:p.Arg961Leu
ENST00000367030.7:c.2882G>T ENSP00000355997.3:p.Arg961Leu
ENST00000391911.5:c.2882G>T ENSP00000375778.1:p.Arg961Leu
ENST00000455193.1:c.89G>T ENSP00000398683.1:p.Arg30Leu
NM_000228.2:c.2882G>T NP_000219.2:p.Arg961Leu
NM_001017402.1:c.2882G>T NP_001017402.1:p.Arg961Leu
NM_001127641.1:c.2882G>T NP_001121113.1:p.Arg961Leu
XM_005273124.3:c.2882G>T XP_005273181.1:p.Arg961Leu
XM_005273124.4:c.2882G>T XP_005273181.1:p.Arg961Leu
XM_017001272.2:c.2690G>T XP_016856761.1:p.Arg897Leu
NM_000228.3:c.2882G>T MANE Select NP_000219.2:p.Arg961Leu
NM_001017402.2:c.2882G>T NP_001017402.1:p.Arg961Leu