Canonical Allele Identifier: CA2170931618
Gene:

Linked Data

dbSNP Id: rs1894672410
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38614798G>T , CM000677.2:g.38614798G>T GRCh38
NC_000015.9:g.38906999G>T , CM000677.1:g.38906999G>T GRCh37
NC_000015.8:g.36694291G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001751736.1:n.281+2343G>T
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