Canonical Allele Identifier: CA1841175620
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551491T= , CM000671.2:g.25551491T= GRCh38
NC_000009.11:g.25551489T= , CM000671.1:g.25551489T= GRCh37
NC_000009.10:g.25541489T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-919A=
XR_929525.2:n.674-919A=