Canonical Allele Identifier: CA36749326

Gene: LAMB3

Linked Data

• dbSNP Id: rs893901753
• MyVariant Identifiers: chr1:g.209790487T>G (hg19) ; chr1:g.209617142T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209617142T>G , CM000663.2:g.209617142T>G	GRCh38
NC_000001.10:g.209790487T>G , CM000663.1:g.209790487T>G	GRCh37
NC_000001.9:g.207857110T>G	NCBI36
NG_007116.1:g.40334A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.3228+268A>C MANE Select	ENSP00000348384.3:n.3228+268A>C
ENST00000356082.8:c.3228+268A>C	ENSP00000348384.3:n.3228+268A>C
ENST00000367030.7:c.3228+268A>C	ENSP00000355997.3:n.3228+268A>C
ENST00000391911.5:c.3228+268A>C	ENSP00000375778.1:n.3228+268A>C
ENST00000455193.1:c.435+268A>C	ENSP00000398683.1:n.435+268A>C
NM_000228.2:c.3228+268A>C	NP_000219.2:n.3228+268A>C
NM_001017402.1:c.3228+268A>C	NP_001017402.1:n.3228+268A>C
NM_001127641.1:c.3228+268A>C	NP_001121113.1:n.3228+268A>C
XM_005273124.3:c.3228+268A>C	XP_005273181.1:n.3228+268A>C
XM_005273124.4:c.3228+268A>C	XP_005273181.1:n.3228+268A>C
XM_017001272.2:c.3036+268A>C	XP_016856761.1:n.3036+268A>C
NM_000228.3:c.3228+268A>C MANE Select	NP_000219.2:n.3228+268A>C
NM_001017402.2:c.3228+268A>C	NP_001017402.1:n.3228+268A>C