Canonical Allele Identifier: CA241233919

Gene: LUM

Linked Data

• dbSNP Id: rs745973307
• gnomAD v2: 12-91505351-TTA-T
• gnomAD v3: 12-91111574-TTA-T
• gnomAD v4: 12-91111574-TTA-T
• MyVariant Identifiers: chr12:g.91505352_91505353del (hg19) ; chr12:g.91111575_91111576del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91111576_91111577del , CM000674.2:g.91111576_91111577del	GRCh38
NC_000012.11:g.91505353_91505354del , CM000674.1:g.91505353_91505354del	GRCh37
NC_000012.10:g.90029484_90029485del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.4:c.-200_-199del	ENSP00000266718.4:n.-200_-199del
NM_002345.3:c.-200_-199del	NP_002336.1:n.-200_-199del