Canonical Allele Identifier: CA1689284812
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13514303G= , CM000669.2:g.13514303G= GRCh38
NC_000007.13:g.13553928G= , CM000669.1:g.13553928G= GRCh37
NC_000007.12:g.13520453G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745097.1:n.148-188013G=