Canonical Allele Identifier: CA423030943

Gene: LAMB3 MIR4260

Linked Data

• MyVariant Identifiers: chr1:g.209796794T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209623449T>A , CM000663.2:g.209623449T>A	GRCh38
NC_000001.10:g.209796794T>A , CM000663.1:g.209796794T>A	GRCh37
NC_000001.9:g.207863417T>A	NCBI36
NG_007116.1:g.34027A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.2358+56A>T (LAMB3) MANE Select	ENSP00000348384.3:n.2358+56A>T
ENST00000356082.8:c.2358+56A>T (LAMB3)	ENSP00000348384.3:n.2358+56A>T
ENST00000367030.7:c.2358+56A>T (LAMB3)	ENSP00000355997.3:n.2358+56A>T
ENST00000391911.5:c.2358+56A>T (LAMB3)	ENSP00000375778.1:n.2358+56A>T
NM_000228.2:c.2358+56A>T (LAMB3)	NP_000219.2:n.2358+56A>T
NM_001017402.1:c.2358+56A>T (LAMB3)	NP_001017402.1:n.2358+56A>T
NM_001127641.1:c.2358+56A>T (LAMB3)	NP_001121113.1:n.2358+56A>T
NR_036213.1:n.62A>T (MIR4260)
XM_005273124.3:c.2358+56A>T (LAMB3)	XP_005273181.1:n.2358+56A>T
XM_005273124.4:c.2358+56A>T (LAMB3)	XP_005273181.1:n.2358+56A>T
XM_017001272.2:c.2166+56A>T (LAMB3)	XP_016856761.1:n.2166+56A>T
NM_000228.3:c.2358+56A>T (LAMB3) MANE Select	NP_000219.2:n.2358+56A>T
NM_001017402.2:c.2358+56A>T (LAMB3)	NP_001017402.1:n.2358+56A>T