Canonical Allele Identifier: CA1672973831
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151627168C= , CM000668.2:g.151627168C= GRCh38
NC_000006.11:g.151948303C= , CM000668.1:g.151948303C= GRCh37
NC_000006.10:g.151989996C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943113.1:n.594C=
XR_943115.1:n.594C=