Canonical Allele Identifier: CA1695966097
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26605805T= , CM000669.2:g.26605805T= GRCh38
NC_000007.13:g.26645424T= , CM000669.1:g.26645424T= GRCh37
NC_000007.12:g.26611949T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927131.1:n.1118-6435A=
XR_927131.2:n.1186-6435A=