Canonical Allele Identifier: CA2551472696
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014527C>T , CM000668.2:g.98014527C>T GRCh38
NC_000006.11:g.98462403C>T , CM000668.1:g.98462403C>T GRCh37
NC_000006.10:g.98569124C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.371+45061C>T
XR_942809.1:n.371+45061C>T