Canonical Allele Identifier: CA1715429914
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69147066G= , CM000669.2:g.69147066G= GRCh38
NC_000007.13:g.68612053G= , CM000669.1:g.68612053G= GRCh37
NC_000007.12:g.68249989G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927647.1:n.88-940C=