Canonical Allele Identifier: CA302041044

Gene: LINC01924

Linked Data

• dbSNP Id: rs113812092
• gnomAD v2: 18-61877165-TG-T
• gnomAD v3: 18-64209930-TG-T
• gnomAD v4: 18-64209930-TG-T
• MyVariant Identifiers: chr18:g.61877166del (hg19) ; chr18:g.64209931del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.64209931del , CM000680.2:g.64209931del	GRCh38
NC_000018.9:g.61877166del , CM000680.1:g.61877166del	GRCh37
NC_000018.8:g.60028146del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033881.1:n.201-39370del