Canonical Allele Identifier: CA2581756078
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21354871G>T , CM000664.2:g.21354871G>T GRCh38
NC_000002.11:g.21577743G>T , CM000664.1:g.21577743G>T GRCh37
NC_000002.10:g.21431248G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939801.2:n.1564-1706G>T