Canonical Allele Identifier: CA138450277
Gene: LINC01512 HGNC NCBI
POLR1C HGNC NCBI

Linked Data

dbSNP Id: rs999296340
gnomAD v2: 6-43904782-G-C
gnomAD v3: 6-43937045-G-C
gnomAD v4: 6-43937045-G-C
MyVariant Identifiers: chr6:g.43904782G>C (hg19) chr6:g.43937045G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43937045G>C , CM000668.2:g.43937045G>C GRCh38
NC_000006.11:g.43904782G>C , CM000668.1:g.43904782G>C GRCh37
NC_000006.10:g.44012760G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024478.1:n.1120G>C (LINC01512)
NM_001318876.2:c.945+407774G>C (POLR1C) NP_001305805.1:n.945+407774G>C
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