Canonical Allele Identifier: CA2206592037
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9581315C= , CM000678.2:g.9581315C= GRCh38
NC_000016.9:g.9675172C= , CM000678.1:g.9675172C= GRCh37
NC_000016.8:g.9582673C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_429665.2:n.1065+14725C=
XR_001752073.1:n.1766+14725C=
XR_001752074.1:n.650+14725C=
XR_001752075.1:n.740+14725C=