Canonical Allele Identifier: CA1678638501
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765665T= , CM000668.2:g.163765665T= GRCh38
NC_000006.11:g.164186697T= , CM000668.1:g.164186697T= GRCh37
NC_000006.10:g.164106687T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6236T=
XR_001744454.1:n.369+6277T=
XR_001744455.1:n.346+6300T=