Canonical Allele Identifier: CA344593520

Gene: LAMB3

Linked Data

• MyVariant Identifiers: chr1:g.209804008T>G (hg19) ; chr1:g.209630663T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209630663T>G , CM000663.2:g.209630663T>G	GRCh38
NC_000001.10:g.209804008T>G , CM000663.1:g.209804008T>G	GRCh37
NC_000001.9:g.207870631T>G	NCBI36
NG_007116.1:g.26813A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.895A>C MANE Select	ENSP00000348384.3:p.Asn299His
ENST00000356082.8:c.895A>C	ENSP00000348384.3:p.Asn299His
ENST00000367030.7:c.895A>C	ENSP00000355997.3:p.Asn299His
ENST00000391911.5:c.895A>C	ENSP00000375778.1:p.Asn299His
NM_000228.2:c.895A>C	NP_000219.2:p.Asn299His
NM_001017402.1:c.895A>C	NP_001017402.1:p.Asn299His
NM_001127641.1:c.895A>C	NP_001121113.1:p.Asn299His
XM_005273124.3:c.895A>C	XP_005273181.1:p.Asn299His
XM_005273124.4:c.895A>C	XP_005273181.1:p.Asn299His
XM_017001272.2:c.703A>C	XP_016856761.1:p.Asn235His
NM_000228.3:c.895A>C MANE Select	NP_000219.2:p.Asn299His
NM_001017402.2:c.895A>C	NP_001017402.1:p.Asn299His