Canonical Allele Identifier: CA1619157059
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439749T= , CM000668.2:g.31439749T= GRCh38
NC_000006.11:g.31407526T= , CM000668.1:g.31407526T= GRCh37
NC_000006.10:g.31515505T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.358A=