Canonical Allele Identifier: CA1094686337

Gene: LINC01312 TARID

Linked Data

• dbSNP Id: rs1774332270
• gnomAD v3: 6-133837589-G-T
• gnomAD v4: 6-133837589-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133837589G>T , CM000668.2:g.133837589G>T	GRCh38
NC_000006.11:g.134158727G>T , CM000668.1:g.134158727G>T	GRCh37
NC_000006.10:g.134200420G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_027030.1:n.590-4G>T (LINC01312)
NR_109982.1:n.478+8288C>A (TARID)