Canonical Allele Identifier: CA36742765

Gene: LAMB3

Linked Data

• dbSNP Id: rs12033066
• gnomAD v2: 1-209788324-G-A
• gnomAD v3: 1-209614979-G-A
• gnomAD v4: 1-209614979-G-A
• MyVariant Identifiers: chr1:g.209788324G>A (hg19) ; chr1:g.209614979G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209614979G>A , CM000663.2:g.209614979G>A	GRCh38
NC_000001.10:g.209788324G>A , CM000663.1:g.209788324G>A	GRCh37
NC_000001.9:g.207854947G>A	NCBI36
NG_007116.1:g.42497C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.*292C>T MANE Select	ENSP00000348384.3:n.*292C>T
ENST00000356082.8:c.*292C>T	ENSP00000348384.3:n.*292C>T
ENST00000367030.7:c.*292C>T	ENSP00000355997.3:n.*292C>T
ENST00000391911.5:c.*292C>T	ENSP00000375778.1:n.*292C>T
NM_000228.2:c.*292C>T	NP_000219.2:n.*292C>T
NM_001017402.1:c.*292C>T	NP_001017402.1:n.*292C>T
NM_001127641.1:c.*292C>T	NP_001121113.1:n.*292C>T
XM_005273124.3:c.*292C>T	XP_005273181.1:n.*292C>T
XM_005273124.4:c.*292C>T	XP_005273181.1:n.*292C>T
XM_017001272.2:c.*292C>T	XP_016856761.1:n.*292C>T
NM_000228.3:c.*292C>T MANE Select	NP_000219.2:n.*292C>T
NM_001017402.2:c.*292C>T	NP_001017402.1:n.*292C>T