Canonical Allele Identifier: CA1648334842
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.95519470C= , CM000668.2:g.95519470C= GRCh38
NC_000006.11:g.95967346C= , CM000668.1:g.95967346C= GRCh37
NC_000006.10:g.96074067C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942795.1:n.96G=