Canonical Allele Identifier: CA2718605850
Gene:

Linked Data

dbSNP Id: rs2129637863
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787425A>T , CM000671.2:g.1787425A>T GRCh38
NC_000009.11:g.1787425A>T , CM000671.1:g.1787425A>T GRCh37
NC_000009.10:g.1777425A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68513A>T
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