Canonical Allele Identifier: CA730844262

Gene: LAMB3

Linked Data

• dbSNP Id: rs1262218588
• MyVariant Identifiers: chr1:g.209788517T>A (hg19) ; chr1:g.209615172T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209615172T>A , CM000663.2:g.209615172T>A	GRCh38
NC_000001.10:g.209788517T>A , CM000663.1:g.209788517T>A	GRCh37
NC_000001.9:g.207855140T>A	NCBI36
NG_007116.1:g.42304A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.*99A>T MANE Select	ENSP00000348384.3:n.*99A>T
ENST00000356082.8:c.*99A>T	ENSP00000348384.3:n.*99A>T
ENST00000367030.7:c.*99A>T	ENSP00000355997.3:n.*99A>T
ENST00000391911.5:c.*99A>T	ENSP00000375778.1:n.*99A>T
NM_000228.2:c.*99A>T	NP_000219.2:n.*99A>T
NM_001017402.1:c.*99A>T	NP_001017402.1:n.*99A>T
NM_001127641.1:c.*99A>T	NP_001121113.1:n.*99A>T
XM_005273124.3:c.*99A>T	XP_005273181.1:n.*99A>T
XM_005273124.4:c.*99A>T	XP_005273181.1:n.*99A>T
XM_017001272.2:c.*99A>T	XP_016856761.1:n.*99A>T
NM_000228.3:c.*99A>T MANE Select	NP_000219.2:n.*99A>T
NM_001017402.2:c.*99A>T	NP_001017402.1:n.*99A>T