Canonical Allele Identifier: CA2206404152
Gene:

Linked Data

dbSNP Id: rs1898214569
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249452C>A , CM000678.2:g.9249452C>A GRCh38
NC_000016.9:g.9343309C>A , CM000678.1:g.9343309C>A GRCh37
NC_000016.8:g.9250810C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64719C>A
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