Canonical Allele Identifier: CA570675833
Gene: LINC01312 HGNC NCBI
TARID HGNC NCBI

Linked Data

dbSNP Id: rs1343770819
gnomAD v2: 6-134158715-C-A
MyVariant Identifiers: chr6:g.134158715C>A (hg19) chr6:g.133837577C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133837577C>A , CM000668.2:g.133837577C>A GRCh38
NC_000006.11:g.134158715C>A , CM000668.1:g.134158715C>A GRCh37
NC_000006.10:g.134200408C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027030.1:n.590-16C>A (LINC01312)
NR_109982.1:n.478+8300G>T (TARID)
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