Canonical Allele Identifier: CA1947280472
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.747022C= , CM000673.2:g.747022C= GRCh38
NC_000011.9:g.747022C= , CM000673.1:g.747022C= GRCh37
NC_000011.8:g.737022C= NCBI36
NG_008160.1:g.4591C=

Transcript Alleles

HGVS Amino-acid change
XR_930963.1:n.259+173C=