Canonical Allele Identifier: CA2526567252
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014447T>C , CM000668.2:g.98014447T>C GRCh38
NC_000006.11:g.98462323T>C , CM000668.1:g.98462323T>C GRCh37
NC_000006.10:g.98569044T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.371+44981T>C
XR_942809.1:n.371+44981T>C