Canonical Allele Identifier: CA2246165611
Gene:

Linked Data

dbSNP Id: rs1598240793
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137289T>A , CM000679.2:g.8137289T>A GRCh38
NC_000017.10:g.8040607T>A , CM000679.1:g.8040607T>A GRCh37
NC_000017.9:g.7981332T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1560T>A
XR_934203.1:n.70-2188T>A
XR_934202.2:n.414-1560T>A
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