Canonical Allele Identifier: CA344585178
Gene: LAMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209618565C>G , CM000663.2:g.209618565C>G GRCh38
NC_000001.10:g.209791910C>G , CM000663.1:g.209791910C>G GRCh37
NC_000001.9:g.207858533C>G NCBI36
NG_007116.1:g.38911G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000356082.9:c.2796G>C MANE Select ENSP00000348384.3:p.Met932Ile
ENST00000356082.8:c.2796G>C ENSP00000348384.3:p.Met932Ile
ENST00000367030.7:c.2796G>C ENSP00000355997.3:p.Met932Ile
ENST00000391911.5:c.2796G>C ENSP00000375778.1:p.Met932Ile
ENST00000455193.1:c.3G>C ENSP00000398683.1:p.Met1Ile
NM_000228.2:c.2796G>C NP_000219.2:p.Met932Ile
NM_001017402.1:c.2796G>C NP_001017402.1:p.Met932Ile
NM_001127641.1:c.2796G>C NP_001121113.1:p.Met932Ile
XM_005273124.3:c.2796G>C XP_005273181.1:p.Met932Ile
XM_005273124.4:c.2796G>C XP_005273181.1:p.Met932Ile
XM_017001272.2:c.2604G>C XP_016856761.1:p.Met868Ile
NM_000228.3:c.2796G>C MANE Select NP_000219.2:p.Met932Ile
NM_001017402.2:c.2796G>C NP_001017402.1:p.Met932Ile