Canonical Allele Identifier: CA709662664

Gene: LINC01147

Linked Data

• dbSNP Id: rs1193613440
• gnomAD v3: 14-88021417-T-C
• gnomAD v4: 14-88021417-T-C
• MyVariant Identifiers: chr14:g.88487761T>C (hg19) ; chr14:g.88021417T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88021417T>C , CM000676.2:g.88021417T>C	GRCh38
NC_000014.8:g.88487761T>C , CM000676.1:g.88487761T>C	GRCh37
NC_000014.7:g.87557514T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110121.1:n.327+2258A>G