Canonical Allele Identifier: CA138465004
Gene: SCIRT HGNC NCBI
POLR1C HGNC NCBI

Linked Data

dbSNP Id: rs1004872544
MyVariant Identifiers: chr6:g.43997359G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43997359G>T , CM000668.2:g.43997359G>T GRCh38
NC_000006.11:g.43965096G>T , CM000668.1:g.43965096G>T GRCh37
NC_000006.10:g.44073074G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125864.1:n.647-51C>A (SCIRT)
NR_125865.1:n.431-51C>A (SCIRT)
NM_001318876.2:c.946-444531G>T (POLR1C) NP_001305805.1:n.946-444531G>T