Canonical Allele Identifier: CA133346615
Gene:

Linked Data

dbSNP Id: rs577421680
MyVariant Identifiers: chr6:g.465931C>T (hg19) chr6:g.465931C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465931C>T , CM000668.2:g.465931C>T GRCh38
NC_000006.11:g.465931C>T , CM000668.1:g.465931C>T GRCh37
NC_000006.10:g.410931C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12206C>T
XR_926365.1:n.2548+12206C>T
XR_001743914.1:n.482-9277C>T
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