Canonical Allele Identifier: CA2293960267
Gene:

Linked Data

dbSNP Id: rs2031435868
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756931G>A , CM000680.2:g.31756931G>A GRCh38
NC_000018.9:g.29336894G>A , CM000680.1:g.29336894G>A GRCh37
NC_000018.8:g.27590892G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5208G>A
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Search 100 bp 3'