Canonical Allele Identifier: CA1912720952
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812978G= , CM000672.2:g.57812978G= GRCh38
NC_000010.10:g.59572738G= , CM000672.1:g.59572738G= GRCh37
NC_000010.9:g.59242744G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34314C=
XR_001747454.1:n.85+34314C=