Canonical Allele Identifier: CA148427346
Gene: LINC01312 HGNC NCBI
TARID HGNC NCBI

Linked Data

dbSNP Id: rs968713270
gnomAD v3: 6-133837594-G-T
gnomAD v4: 6-133837594-G-T
MyVariant Identifiers: chr6:g.134158732G>T (hg19) chr6:g.133837594G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133837594G>T , CM000668.2:g.133837594G>T GRCh38
NC_000006.11:g.134158732G>T , CM000668.1:g.134158732G>T GRCh37
NC_000006.10:g.134200425G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027030.1:n.591G>T (LINC01312)
NR_109982.1:n.478+8283C>A (TARID)
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