Canonical Allele Identifier: CA1760508094
Gene:

Linked Data

dbSNP Id: rs1798588633
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907812T>A , CM000670.2:g.5907812T>A GRCh38
NC_000008.10:g.5765334T>A , CM000670.1:g.5765334T>A GRCh37
NC_000008.9:g.5752742T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941374.1:n.308-8081A>T
XR_941375.1:n.308-8081A>T
XR_941376.1:n.406-8081A>T
XR_941377.1:n.308-8081A>T
XR_941378.1:n.216-8081A>T
XR_001745765.1:n.308-8081A>T
XR_001745766.1:n.406-8081A>T
XR_001745767.1:n.216-8081A>T
XR_001745768.1:n.308-8081A>T
XR_941374.2:n.308-8081A>T
XR_941375.2:n.308-8081A>T
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