Canonical Allele Identifier: CA2574003626

Gene: LAMB3

Linked Data

• gnomAD v4: 1-209630548-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209630548A>G , CM000663.2:g.209630548A>G	GRCh38
NC_000001.10:g.209803893A>G , CM000663.1:g.209803893A>G	GRCh37
NC_000001.9:g.207870516A>G	NCBI36
NG_007116.1:g.26928T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.943+67T>C MANE Select	ENSP00000348384.3:n.943+67T>C
ENST00000356082.8:c.943+67T>C	ENSP00000348384.3:n.943+67T>C
ENST00000367030.7:c.943+67T>C	ENSP00000355997.3:n.943+67T>C
ENST00000391911.5:c.943+67T>C	ENSP00000375778.1:n.943+67T>C
NM_000228.2:c.943+67T>C	NP_000219.2:n.943+67T>C
NM_001017402.1:c.943+67T>C	NP_001017402.1:n.943+67T>C
NM_001127641.1:c.943+67T>C	NP_001121113.1:n.943+67T>C
XM_005273124.3:c.943+67T>C	XP_005273181.1:n.943+67T>C
XM_005273124.4:c.943+67T>C	XP_005273181.1:n.943+67T>C
XM_017001272.2:c.751+67T>C	XP_016856761.1:n.751+67T>C
NM_000228.3:c.943+67T>C MANE Select	NP_000219.2:n.943+67T>C
NM_001017402.2:c.943+67T>C	NP_001017402.1:n.943+67T>C