Canonical Allele Identifier: CA197961767

Gene: LINC01492

Linked Data

• dbSNP Id: rs376488982
• gnomAD v2: 9-106024068-CAT-C
• gnomAD v3: 9-103261786-CAT-C
• gnomAD v4: 9-103261786-CAT-C
• MyVariant Identifiers: chr9:g.106024069_106024070del (hg19) ; chr9:g.103261787_103261788del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261787_103261788del , CM000671.2:g.103261787_103261788del	GRCh38
NC_000009.11:g.106024069_106024070del , CM000671.1:g.106024069_106024070del	GRCh37
NC_000009.10:g.105063890_105063891del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2736_771+2737del