Canonical Allele Identifier: CA265472424

Gene: LINC01147

Linked Data

• dbSNP Id: rs1028322017
• gnomAD v2: 14-88487745-A-C
• gnomAD v3: 14-88021401-A-C
• gnomAD v4: 14-88021401-A-C
• MyVariant Identifiers: chr14:g.88487745A>C (hg19) ; chr14:g.88021401A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88021401A>C , CM000676.2:g.88021401A>C	GRCh38
NC_000014.8:g.88487745A>C , CM000676.1:g.88487745A>C	GRCh37
NC_000014.7:g.87557498A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110121.1:n.327+2274T>G