Canonical Allele Identifier: CA2484300825

Gene: LAMB3

Linked Data

• dbSNP Id: rs1666600301
• gnomAD v4: 1-209629639-G-GCA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209629639_209629640insCA , CM000663.2:g.209629639_209629640insCA	GRCh38
NC_000001.10:g.209802984_209802985insCA , CM000663.1:g.209802984_209802985insCA	GRCh37
NC_000001.9:g.207869607_207869608insCA	NCBI36
NG_007116.1:g.27836_27837insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1132+97_1132+98insTG MANE Select	ENSP00000348384.3:n.1132+97_1132+98insTG
ENST00000356082.8:c.1132+97_1132+98insTG	ENSP00000348384.3:n.1132+97_1132+98insTG
ENST00000367030.7:c.1132+97_1132+98insTG	ENSP00000355997.3:n.1132+97_1132+98insTG
ENST00000391911.5:c.1132+97_1132+98insTG	ENSP00000375778.1:n.1132+97_1132+98insTG
NM_000228.2:c.1132+97_1132+98insTG	NP_000219.2:n.1132+97_1132+98insTG
NM_001017402.1:c.1132+97_1132+98insTG	NP_001017402.1:n.1132+97_1132+98insTG
NM_001127641.1:c.1132+97_1132+98insTG	NP_001121113.1:n.1132+97_1132+98insTG
XM_005273124.3:c.1132+97_1132+98insTG	XP_005273181.1:n.1132+97_1132+98insTG
XM_005273124.4:c.1132+97_1132+98insTG	XP_005273181.1:n.1132+97_1132+98insTG
XM_017001272.2:c.940+97_940+98insTG	XP_016856761.1:n.940+97_940+98insTG
NM_000228.3:c.1132+97_1132+98insTG MANE Select	NP_000219.2:n.1132+97_1132+98insTG
NM_001017402.2:c.1132+97_1132+98insTG	NP_001017402.1:n.1132+97_1132+98insTG