Canonical Allele Identifier: CA2517821502
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41648328G>C , CM000681.2:g.41648328G>C GRCh38
NC_000019.9:g.42152249G>C , CM000681.1:g.42152249G>C GRCh37
NC_000019.8:g.46844089G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935972.1:n.170+3174C>G