Canonical Allele Identifier: CA1841175396
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551100A= , CM000671.2:g.25551100A= GRCh38
NC_000009.11:g.25551098A= , CM000671.1:g.25551098A= GRCh37
NC_000009.10:g.25541098A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-528T=
XR_929525.2:n.674-528T=