Canonical Allele Identifier: CA2569499694
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014480C>T , CM000668.2:g.98014480C>T GRCh38
NC_000006.11:g.98462356C>T , CM000668.1:g.98462356C>T GRCh37
NC_000006.10:g.98569077C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.371+45014C>T
XR_942809.1:n.371+45014C>T