Canonical Allele Identifier: CA2713161406
Gene:

Linked Data

dbSNP Id: rs1461610652
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633786T>G , CM000668.2:g.151633786T>G GRCh38
NC_000006.11:g.151954921T>G , CM000668.1:g.151954921T>G GRCh37
NC_000006.10:g.151996614T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3804T>G
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