Canonical Allele Identifier: CA1205766005
Gene:

Linked Data

dbSNP Id: rs1648345442
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649408A>G , CM000663.2:g.168649408A>G GRCh38
NC_000001.10:g.168618646A>G , CM000663.1:g.168618646A>G GRCh37
NC_000001.9:g.166885270A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-8133T>C
XR_922259.2:n.332-8133T>C
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