Canonical Allele Identifier: CA1841175449
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551208C= , CM000671.2:g.25551208C= GRCh38
NC_000009.11:g.25551206C= , CM000671.1:g.25551206C= GRCh37
NC_000009.10:g.25541206C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-636G=
XR_929525.2:n.674-636G=