Canonical Allele Identifier: CA133346567
Gene:

Linked Data

dbSNP Id: rs962342078
MyVariant Identifiers: chr6:g.465898A>C (hg19) chr6:g.465898A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465898A>C , CM000668.2:g.465898A>C GRCh38
NC_000006.11:g.465898A>C , CM000668.1:g.465898A>C GRCh37
NC_000006.10:g.410898A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12173A>C
XR_926365.1:n.2548+12173A>C
XR_001743914.1:n.482-9310A>C
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