Canonical Allele Identifier: CA589962176

Gene: LINC01492

Linked Data

• dbSNP Id: rs1281029568
• gnomAD v2: 9-106024015-TC-T
• gnomAD v3: 9-103261733-TC-T
• gnomAD v4: 9-103261733-TC-T
• MyVariant Identifiers: chr9:g.106024016del (hg19) ; chr9:g.103261734del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261734del , CM000671.2:g.103261734del	GRCh38
NC_000009.11:g.106024016del , CM000671.1:g.106024016del	GRCh37
NC_000009.10:g.105063837del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2790del