Canonical Allele Identifier: CA1649498161
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014576A= , CM000668.2:g.98014576A= GRCh38
NC_000006.11:g.98462452A= , CM000668.1:g.98462452A= GRCh37
NC_000006.10:g.98569173A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.371+45110A=
XR_942809.1:n.371+45110A=