Canonical Allele Identifier: CA1608913938
Gene:

Linked Data

dbSNP Id: rs1759194584
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169727C>A , CM000668.2:g.8169727C>A GRCh38
NC_000006.11:g.8169960C>A , CM000668.1:g.8169960C>A GRCh37
NC_000006.10:g.8114959C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11467C>A
XR_926441.1:n.189+1807C>A
XR_926442.1:n.82+11467C>A
XR_926443.1:n.82+11467C>A
XR_001743950.1:n.179+1807C>A
XR_926440.2:n.74+11467C>A
XR_926441.2:n.179+1807C>A
XR_926443.2:n.83+11467C>A
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