Canonical Allele Identifier: CA1672973829
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151627160A= , CM000668.2:g.151627160A= GRCh38
NC_000006.11:g.151948295A= , CM000668.1:g.151948295A= GRCh37
NC_000006.10:g.151989988A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943113.1:n.586A=
XR_943115.1:n.586A=