Canonical Allele Identifier: CA2840504481
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787705C>T , CM000671.2:g.1787705C>T GRCh38
NC_000009.11:g.1787705C>T , CM000671.1:g.1787705C>T GRCh37
NC_000009.10:g.1777705C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68793C>T