Canonical Allele Identifier: CA1985859949
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.80851703T= , CM000673.2:g.80851703T= GRCh38
NC_000011.9:g.80562746T= , CM000673.1:g.80562746T= GRCh37
NC_000011.8:g.80240394T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247272.2:n.124+60588A=