Canonical Allele Identifier: CA1011766255

Gene: LAMB3

Linked Data

• dbSNP Id: rs1666084691
• gnomAD v3: 1-209618757-G-C
• gnomAD v4: 1-209618757-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209618757G>C , CM000663.2:g.209618757G>C	GRCh38
NC_000001.10:g.209792102G>C , CM000663.1:g.209792102G>C	GRCh37
NC_000001.9:g.207858725G>C	NCBI36
NG_007116.1:g.38719C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.2702-98C>G MANE Select	ENSP00000348384.3:n.2702-98C>G
ENST00000356082.8:c.2702-98C>G	ENSP00000348384.3:n.2702-98C>G
ENST00000367030.7:c.2702-98C>G	ENSP00000355997.3:n.2702-98C>G
ENST00000391911.5:c.2702-98C>G	ENSP00000375778.1:n.2702-98C>G
ENST00000455193.1:c.-190C>G	ENSP00000398683.1:n.-190C>G
NM_000228.2:c.2702-98C>G	NP_000219.2:n.2702-98C>G
NM_001017402.1:c.2702-98C>G	NP_001017402.1:n.2702-98C>G
NM_001127641.1:c.2702-98C>G	NP_001121113.1:n.2702-98C>G
XM_005273124.3:c.2702-98C>G	XP_005273181.1:n.2702-98C>G
XM_005273124.4:c.2702-98C>G	XP_005273181.1:n.2702-98C>G
XM_017001272.2:c.2510-98C>G	XP_016856761.1:n.2510-98C>G
NM_000228.3:c.2702-98C>G MANE Select	NP_000219.2:n.2702-98C>G
NM_001017402.2:c.2702-98C>G	NP_001017402.1:n.2702-98C>G