Canonical Allele Identifier: CA2711022590
Gene:

Linked Data

dbSNP Id: rs2113750187
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8228601T>A , CM000668.2:g.8228601T>A GRCh38
NC_000006.11:g.8228834T>A , CM000668.1:g.8228834T>A GRCh37
NC_000006.10:g.8173833T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.83-1513T>A
XR_926441.1:n.190-10330T>A
XR_926442.1:n.83-1513T>A
XR_926443.1:n.83-10330T>A
XR_001743950.1:n.180-10330T>A
XR_926440.2:n.75-1513T>A
XR_926441.2:n.180-10330T>A
XR_926443.2:n.84-10330T>A
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