Canonical Allele Identifier: CA344592727

Gene: LAMB3

Linked Data

• MyVariant Identifiers: chr1:g.209803222A>G (hg19) ; chr1:g.209629877A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209629877A>G , CM000663.2:g.209629877A>G	GRCh38
NC_000001.10:g.209803222A>G , CM000663.1:g.209803222A>G	GRCh37
NC_000001.9:g.207869845A>G	NCBI36
NG_007116.1:g.27599T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.992T>C MANE Select	ENSP00000348384.3:p.Val331Ala
ENST00000356082.8:c.992T>C	ENSP00000348384.3:p.Val331Ala
ENST00000367030.7:c.992T>C	ENSP00000355997.3:p.Val331Ala
ENST00000391911.5:c.992T>C	ENSP00000375778.1:p.Val331Ala
NM_000228.2:c.992T>C	NP_000219.2:p.Val331Ala
NM_001017402.1:c.992T>C	NP_001017402.1:p.Val331Ala
NM_001127641.1:c.992T>C	NP_001121113.1:p.Val331Ala
XM_005273124.3:c.992T>C	XP_005273181.1:p.Val331Ala
XM_005273124.4:c.992T>C	XP_005273181.1:p.Val331Ala
XM_017001272.2:c.800T>C	XP_016856761.1:p.Val267Ala
NM_000228.3:c.992T>C MANE Select	NP_000219.2:p.Val331Ala
NM_001017402.2:c.992T>C	NP_001017402.1:p.Val331Ala