Canonical Allele Identifier: CA1644769188
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87942862T= , CM000668.2:g.87942862T= GRCh38
NC_000006.11:g.88652580T= , CM000668.1:g.88652580T= GRCh37
NC_000006.10:g.88709299T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001744246.1:n.1581T=