Canonical Allele Identifier: CA197961754

Gene: LINC01492

Linked Data

• dbSNP Id: rs948715961
• gnomAD v3: 9-103261747-GC-G
• gnomAD v4: 9-103261747-GC-G
• MyVariant Identifiers: chr9:g.106024030del (hg19) ; chr9:g.103261748del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261748del , CM000671.2:g.103261748del	GRCh38
NC_000009.11:g.106024030del , CM000671.1:g.106024030del	GRCh37
NC_000009.10:g.105063851del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2776del