Canonical Allele Identifier: CA138450278
Gene: LINC01512 HGNC NCBI
POLR1C HGNC NCBI

Linked Data

dbSNP Id: rs1033002658
gnomAD v2: 6-43904793-C-A
gnomAD v3: 6-43937056-C-A
gnomAD v4: 6-43937056-C-A
MyVariant Identifiers: chr6:g.43904793C>A (hg19) chr6:g.43937056C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43937056C>A , CM000668.2:g.43937056C>A GRCh38
NC_000006.11:g.43904793C>A , CM000668.1:g.43904793C>A GRCh37
NC_000006.10:g.44012771C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024478.1:n.1131C>A (LINC01512)
NM_001318876.2:c.945+407785C>A (POLR1C) NP_001305805.1:n.945+407785C>A
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