Canonical Allele Identifier: CA646385646

Gene: LAMB3

Linked Data

• COSMIC: COSN22396551

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209614988A>C , CM000663.2:g.209614988A>C	GRCh38
NC_000001.10:g.209788333A>C , CM000663.1:g.209788333A>C	GRCh37
NC_000001.9:g.207854956A>C	NCBI36
NG_007116.1:g.42488T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.*283T>G MANE Select	ENSP00000348384.3:n.*283T>G
ENST00000356082.8:c.*283T>G	ENSP00000348384.3:n.*283T>G
ENST00000367030.7:c.*283T>G	ENSP00000355997.3:n.*283T>G
ENST00000391911.5:c.*283T>G	ENSP00000375778.1:n.*283T>G
NM_000228.2:c.*283T>G	NP_000219.2:n.*283T>G
NM_001017402.1:c.*283T>G	NP_001017402.1:n.*283T>G
NM_001127641.1:c.*283T>G	NP_001121113.1:n.*283T>G
XM_005273124.3:c.*283T>G	XP_005273181.1:n.*283T>G
XM_005273124.4:c.*283T>G	XP_005273181.1:n.*283T>G
XM_017001272.2:c.*283T>G	XP_016856761.1:n.*283T>G
NM_000228.3:c.*283T>G MANE Select	NP_000219.2:n.*283T>G
NM_001017402.2:c.*283T>G	NP_001017402.1:n.*283T>G