Canonical Allele Identifier: CA709662592

Gene: LINC01147

Linked Data

• dbSNP Id: rs1172248064
• MyVariant Identifiers: chr14:g.88487655C>G (hg19) ; chr14:g.88021311C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88021311C>G , CM000676.2:g.88021311C>G	GRCh38
NC_000014.8:g.88487655C>G , CM000676.1:g.88487655C>G	GRCh37
NC_000014.7:g.87557408C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110121.1:n.327+2364G>C