Canonical Allele Identifier: CA828760853
Gene:

Linked Data

dbSNP Id: rs1291091053
MyVariant Identifiers: chr6:g.8228852T>C (hg19) chr6:g.8228619T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8228619T>C , CM000668.2:g.8228619T>C GRCh38
NC_000006.11:g.8228852T>C , CM000668.1:g.8228852T>C GRCh37
NC_000006.10:g.8173851T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.83-1495T>C
XR_926441.1:n.190-10312T>C
XR_926442.1:n.83-1495T>C
XR_926443.1:n.83-10312T>C
XR_001743950.1:n.180-10312T>C
XR_926440.2:n.75-1495T>C
XR_926441.2:n.180-10312T>C
XR_926443.2:n.84-10312T>C
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