Canonical Allele Identifier: CA1678638459
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765583C= , CM000668.2:g.163765583C= GRCh38
NC_000006.11:g.164186615C= , CM000668.1:g.164186615C= GRCh37
NC_000006.10:g.164106605C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001744452.1:n.410+6154C=
XR_001744454.1:n.369+6195C=
XR_001744455.1:n.346+6218C=