Canonical Allele Identifier: CA1649498154
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014565C= , CM000668.2:g.98014565C= GRCh38
NC_000006.11:g.98462441C= , CM000668.1:g.98462441C= GRCh37
NC_000006.10:g.98569162C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.371+45099C=
XR_942809.1:n.371+45099C=