Canonical Allele Identifier: CA1619157193
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31440092T= , CM000668.2:g.31440092T= GRCh38
NC_000006.11:g.31407869T= , CM000668.1:g.31407869T= GRCh37
NC_000006.10:g.31515848T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.55-40A=