Canonical Allele Identifier: CA1011766264

Gene: LAMB3

Linked Data

• dbSNP Id: rs1666088724
• gnomAD v3: 1-209618883-GGGA-G
• gnomAD v4: 1-209618883-GGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209618892_209618894del , CM000663.2:g.209618892_209618894del	GRCh38
NC_000001.10:g.209792237_209792239del , CM000663.1:g.209792237_209792239del	GRCh37
NC_000001.9:g.207858860_207858862del	NCBI36
NG_007116.1:g.38590_38592del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.2702-227_2702-225del MANE Select	ENSP00000348384.3:n.2702-227_2702-225del
ENST00000356082.8:c.2702-227_2702-225del	ENSP00000348384.3:n.2702-227_2702-225del
ENST00000367030.7:c.2702-227_2702-225del	ENSP00000355997.3:n.2702-227_2702-225del
ENST00000391911.5:c.2702-227_2702-225del	ENSP00000375778.1:n.2702-227_2702-225del
NM_000228.2:c.2702-227_2702-225del	NP_000219.2:n.2702-227_2702-225del
NM_001017402.1:c.2702-227_2702-225del	NP_001017402.1:n.2702-227_2702-225del
NM_001127641.1:c.2702-227_2702-225del	NP_001121113.1:n.2702-227_2702-225del
XM_005273124.3:c.2702-227_2702-225del	XP_005273181.1:n.2702-227_2702-225del
XM_005273124.4:c.2702-227_2702-225del	XP_005273181.1:n.2702-227_2702-225del
XM_017001272.2:c.2510-227_2510-225del	XP_016856761.1:n.2510-227_2510-225del
NM_000228.3:c.2702-227_2702-225del MANE Select	NP_000219.2:n.2702-227_2702-225del
NM_001017402.2:c.2702-227_2702-225del	NP_001017402.1:n.2702-227_2702-225del