Canonical Allele Identifier: CA344580494
Gene: LAMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209615277G>C , CM000663.2:g.209615277G>C GRCh38
NC_000001.10:g.209788622G>C , CM000663.1:g.209788622G>C GRCh37
NC_000001.9:g.207855245G>C NCBI36
NG_007116.1:g.42199C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000356082.9:c.3513C>G MANE Select ENSP00000348384.3:p.Cys1171Trp
ENST00000356082.8:c.3513C>G ENSP00000348384.3:p.Cys1171Trp
ENST00000367030.7:c.3513C>G ENSP00000355997.3:p.Cys1171Trp
ENST00000391911.5:c.3513C>G ENSP00000375778.1:p.Cys1171Trp
NM_000228.2:c.3513C>G NP_000219.2:p.Cys1171Trp
NM_001017402.1:c.3513C>G NP_001017402.1:p.Cys1171Trp
NM_001127641.1:c.3513C>G NP_001121113.1:p.Cys1171Trp
XM_005273124.3:c.3513C>G XP_005273181.1:p.Cys1171Trp
XM_005273124.4:c.3513C>G XP_005273181.1:p.Cys1171Trp
XM_017001272.2:c.3321C>G XP_016856761.1:p.Cys1107Trp
NM_000228.3:c.3513C>G MANE Select NP_000219.2:p.Cys1171Trp
NM_001017402.2:c.3513C>G NP_001017402.1:p.Cys1171Trp