Canonical Allele Identifier: CA1841175558
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551398T= , CM000671.2:g.25551398T= GRCh38
NC_000009.11:g.25551396T= , CM000671.1:g.25551396T= GRCh37
NC_000009.10:g.25541396T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-826A=
XR_929525.2:n.674-826A=