Canonical Allele Identifier: CA1619157211
Gene:

Linked Data

dbSNP Id: rs1761797744
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31440170C>A , CM000668.2:g.31440170C>A GRCh38
NC_000006.11:g.31407947C>A , CM000668.1:g.31407947C>A GRCh37
NC_000006.10:g.31515926C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.55-118G>T
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