Canonical Allele Identifier: CA823881998
Gene:

Linked Data

dbSNP Id: rs9469002
MyVariant Identifiers: chr6:g.31407772G>A (hg19) chr6:g.31439995G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439995G>A , CM000668.2:g.31439995G>A GRCh38
NC_000006.11:g.31407772G>A , CM000668.1:g.31407772G>A GRCh37
NC_000006.10:g.31515751G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.112C>T
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