Canonical Allele Identifier: CA1870932961
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092836C= , CM000671.2:g.108092836C= GRCh38
NC_000009.11:g.110855117C= , CM000671.1:g.110855117C= GRCh37
NC_000009.10:g.109894938C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930239.1:n.461-39542G=
XR_001746881.1:n.668-39542G=
XR_001746882.1:n.668-39542G=